HBG2 NM_000184.2:c.-211C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position -211 in the upstream promoter region of the HBG2 gene where cytosine has been mutated to thymine.

**Synonyms:** - Ggamma -158C>T - HBG2 (XmnI) - rs7482144 C>T - HBG2 Promoter SNP (g. -158C>T) - HBG2 XmnI C>T Polymorphism - HBG2 c.-211C>T - HBG2, C-T, -158 - Hemoglobin Subunit Gamma 2 c.-211C>T - Hemoglobin, Gamma G c.-211C>T - NG_000007.3:g.42677C>T - NG_042299.1:g.1053G>A - NM_000184.2:c.-211C>T - Xmn1-HBG2 SNP C>T