Hemoglobin A

HematologyAlso known as: HbAAlso known as: Hemoglobin A1[arb'U]/mL

Quantifies the percentage of normal adult hemoglobin (HbA) in blood.

Normal Range
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[arb'U]/mL
Abnormal Levels
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Specimen Type
Blood

Why This Biomarker Matters

Identifies hemoglobin variants and inherited blood disorders. Abnormal percentages indicate sickle cell disease, thalassemia, or other conditions requiring monitoring and treatment.

Overview

Hemoglobin A (HbA) is the normal predominant form of hemoglobin in adult red blood cells, making up about 95-98% of total hemoglobin. This test quantifies HbA percentage using electrophoresis. Hemoglobin electrophoresis separates different hemoglobin types to screen for disorders like sickle cell disease, thalassemia, and other hemoglobinopathies. Low HbA percentage indicates abnormal hemoglobin variants are present. This test is essential for diagnosing inherited blood disorders, especially in at-risk populations, and is often performed on newborns as part of screening programs.

Technical Information (LOINC Codes)

Standardized laboratory codes for this biomarker

10346-5Primary
Hemoglobin A [Units/volume] in Blood by Electrophoresis
[arb'U]/mL
45208-6
Hemoglobin A [Presence] in Blood by Electrophoresis

Available Lab Tests

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