Canonical Allele Identifier: CA467852734

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131335G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255948G>C , CM000671.2:g.133255948G>C	GRCh38
NC_000009.11:g.136131335G>C , CM000671.1:g.136131335G>C	GRCh37
NC_000009.10:g.135121156G>C	NCBI36
NG_006669.1:g.21720C>G
NG_006669.2:g.24268C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.812C>G
ENST00000647353.1:n.54-4796C>G
ENST00000679909.1:c.28+19214C>G	ENSP00000506089.1:n.28+19214C>G
ENST00000453660.3:n.794C>G
ENST00000538324.2:c.780C>G	ENSP00000483018.1:p.Gly260=
ENST00000611156.4:c.780C>G	ENSP00000483265.1:p.Gly260=
NM_020469.2:c.783C>G	NP_065202.2:p.Gly261=
NM_020469.3:c.783C>G	NP_065202.2:p.Gly261=