Canonical Allele Identifier: CA375686800

Gene: ABO

Linked Data

• gnomAD v4: 9-133257538-T-C
• MyVariant Identifiers: chr9:g.136132925T>C (hg19) ; chr9:g.133257538T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257538T>C , CM000671.2:g.133257538T>C	GRCh38
NC_000009.11:g.136132925T>C , CM000671.1:g.136132925T>C	GRCh37
NC_000009.10:g.135122746T>C	NCBI36
NG_006669.1:g.20129A>G
NG_006669.2:g.22677A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.274A>G
ENST00000647353.1:n.54-6386A>G
ENST00000651471.1:n.329+504A>G
ENST00000679909.1:c.28+17624A>G	ENSP00000506089.1:n.28+17624A>G
ENST00000453660.3:n.256A>G
ENST00000538324.2:c.244A>G	ENSP00000483018.1:p.Lys82Glu
ENST00000611156.4:c.244A>G	ENSP00000483265.1:p.Lys82Glu
NM_020469.2:c.244A>G	NP_065202.2:p.Lys82Glu
NM_020469.3:c.244A>G	NP_065202.2:p.Lys82Glu