Canonical Allele Identifier: CA1882579256

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255677G= , CM000671.2:g.133255677G=	GRCh38
NC_000009.11:g.136131064G= , CM000671.1:g.136131064G=	GRCh37
NC_000009.10:g.135120885G=	NCBI36
NG_006669.1:g.21991C=
NG_006669.2:g.24539C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1083C=
ENST00000647353.1:n.54-4525C=
ENST00000679909.1:c.28+19485C=	ENSP00000506089.1:n.28+19485C=
ENST00000453660.3:n.1065C=
ENST00000538324.2:c.1051C=	ENSP00000483018.1:p.Arg351=
ENST00000611156.4:c.1051C=	ENSP00000483265.1:p.Arg351=
NM_020469.2:c.1054C=	NP_065202.2:p.Arg352=
NM_020469.3:c.1054C=	NP_065202.2:p.Arg352=