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Hemoglobin Electrophoresis, Whole Blood — Qualitative

Published: August 9, 2026Updated: August 16, 2026

A whole-blood test that separates hemoglobin types to help identify variants such as sickle cell disease, thalassemia, or other inherited hemoglobin disorders.

Quick summary

["This test helps determine whether an unusual hemoglobin type may be present."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
4613-6
Short code
Hgb N-Balt Bld Ql Elph Acid
Synonyms
Hgb N-Balt Bld Ql Elph Acid
Category
liver
Sample
whole-blood
Container
Lavender-top (EDTA)
Units
N/A
Ref low
7
Ref high
56
Critical range
7 N/A – 20 N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Method
electrophoresis-ph
CPT
84484
SNOMED
302773008
Specimen volume
3 mL
Stability
Room temperature: 4h, Refrigerated: 24h
Hemolysis max
0
Lipemia max
0
Icterus max
0
TAT
4–24 hours
Order
routine

What is this test?

Hemoglobin electrophoresis is a laboratory test that separates different forms of hemoglobin so they can be identified. It is commonly used to evaluate suspected sickle cell disease, thalassemia, and other inherited hemoglobin conditions.

Why might I need this test?

Your clinician may order this test after an abnormal blood count, a physical examination suggesting a blood disorder, screening results, or a family history of an inherited hemoglobin condition. It may also be used to confirm the type of an abnormal hemoglobin finding.

How is the test performed?

A small blood sample is collected from a vein, usually in the arm. The laboratory processes the sample using electrophoresis to measure and identify different hemoglobin forms. Additional genetic testing may be needed if the result is unclear.

How do I prepare for the test?

No fasting or special preparation is usually necessary. Tell your clinician if you have recently received a blood transfusion, because donor red blood cells can affect the interpretation of the results.

Reference range

Adult males: 7-56 U/L; Adult females: 7-43 U/LN/A

Specimen: whole-blood

No special preparation required. Avoid fatty meals before the test if possible.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

An abnormal electrophoresis pattern may indicate a hemoglobin variant, thalassemia, sickle cell disease, or another inherited blood condition. Some variants are benign, while others can cause anemia or other health problems. Results should be interpreted with your blood count, medical history, and other laboratory tests by your clinician.

Short name

Hemoglobin electrophoresis

Frequently asked questions

Does this test diagnose sickle cell disease or thalassemia?
It can identify or suggest these conditions, but the diagnosis may also require blood counts, genetic testing, and clinical evaluation.
Does a normal result rule out every inherited blood disorder?
No. Some hemoglobin variants may not be detected by electrophoresis, so additional testing may be needed when clinical findings strongly suggest a blood disorder.
Can I take this test if I recently had a blood transfusion?
Yes, but tell your clinician about the transfusion because it may change the results and make interpretation less straightforward.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy