Canonical Allele Identifier: CA1882580292

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256082G= , CM000671.2:g.133256082G=	GRCh38
NC_000009.11:g.136131469G= , CM000671.1:g.136131469G=	GRCh37
NC_000009.10:g.135121290G=	NCBI36
NG_006669.1:g.21586C=
NG_006669.2:g.24134C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.678C=
ENST00000647353.1:n.54-4930C=
ENST00000679909.1:c.28+19080C=	ENSP00000506089.1:n.28+19080C=
ENST00000453660.3:n.660C=
ENST00000538324.2:c.646C=	ENSP00000483018.1:p.Arg216=
ENST00000611156.4:c.646C=	ENSP00000483265.1:p.Arg216=
NM_020469.2:c.649C=	NP_065202.2:p.Arg217=
NM_020469.3:c.649C=	NP_065202.2:p.Arg217=