Canonical Allele Identifier: CA1882579469

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255767C= , CM000671.2:g.133255767C=	GRCh38
NC_000009.11:g.136131154C= , CM000671.1:g.136131154C=	GRCh37
NC_000009.10:g.135120975C=	NCBI36
NG_006669.1:g.21901G=
NG_006669.2:g.24449G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.993G=
ENST00000647353.1:n.54-4615G=
ENST00000679909.1:c.28+19395G=	ENSP00000506089.1:n.28+19395G=
ENST00000453660.3:n.975G=
ENST00000538324.2:c.961G=	ENSP00000483018.1:p.Glu321=
ENST00000611156.4:c.961G=	ENSP00000483265.1:p.Glu321=
NM_020469.2:c.964G=	NP_065202.2:p.Glu322=
NM_020469.3:c.964G=	NP_065202.2:p.Glu322=