Canonical Allele Identifier: CA467852844

Gene: ABO

Linked Data

• dbSNP Id: rs1268227721
• gnomAD v2: 9-136131404-T-C
• MyVariant Identifiers: chr9:g.136131404T>C (hg19) ; chr9:g.133256017T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256017T>C , CM000671.2:g.133256017T>C	GRCh38
NC_000009.11:g.136131404T>C , CM000671.1:g.136131404T>C	GRCh37
NC_000009.10:g.135121225T>C	NCBI36
NG_006669.1:g.21651A>G
NG_006669.2:g.24199A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.743A>G
ENST00000647353.1:n.54-4865A>G
ENST00000679909.1:c.28+19145A>G	ENSP00000506089.1:n.28+19145A>G
ENST00000453660.3:n.725A>G
ENST00000538324.2:c.711A>G	ENSP00000483018.1:p.Gly237=
ENST00000611156.4:c.711A>G	ENSP00000483265.1:p.Gly237=
NM_020469.2:c.714A>G	NP_065202.2:p.Gly238=
NM_020469.3:c.714A>G	NP_065202.2:p.Gly238=