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What is Hemoglobin AA?

Published in Hemoglobin Genotypes 2 mins read

Hemoglobin AA refers to normal hemoglobin, which occurs when a person inherits a Hemoglobin A gene from each parent.

Here's a breakdown:

  • Hemoglobin A: This is the standard, healthy form of hemoglobin found in most individuals.
  • Inheritance: We inherit genes from both our parents.
  • AA Genotype: Having the AA genotype means inheriting the Hemoglobin A gene from both parents.

Understanding Hemoglobin Genotypes

To better understand Hemoglobin AA, it's helpful to consider other possible hemoglobin genotypes. The reference text mentions Hemoglobin S and Hemoglobin C as possible changes to normal hemoglobin. Here's a table summarizing different genotypes:

Genotype Description
AA Normal Hemoglobin: Inheriting a Hemoglobin A gene from each parent.
AS Carrier of Sickle Cell Trait: Inheriting a Hemoglobin A gene from one parent and a Hemoglobin S from the other.
AC Carrier of Hemoglobin C Trait: Inheriting a Hemoglobin A gene from one parent and a Hemoglobin C from the other.
SS Sickle Cell Anemia: Inheriting a Hemoglobin S gene from each parent.
SC Compound Heterozygote: Inheriting a Hemoglobin S gene from one parent and a Hemoglobin C from the other.
CC Hemoglobin C Disease: Inheriting a Hemoglobin C gene from each parent.

Key Takeaway

If you have Hemoglobin AA, you have the normal, healthy version of hemoglobin.

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