Canonical Allele Identifier: CA1882579387

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255732G= , CM000671.2:g.133255732G=	GRCh38
NC_000009.11:g.136131119G= , CM000671.1:g.136131119G=	GRCh37
NC_000009.10:g.135120940G=	NCBI36
NG_006669.1:g.21936C=
NG_006669.2:g.24484C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1028C=
ENST00000647353.1:n.54-4580C=
ENST00000679909.1:c.28+19430C=	ENSP00000506089.1:n.28+19430C=
ENST00000453660.3:n.1010C=
ENST00000538324.2:c.996C=	ENSP00000483018.1:p.Pro332=
ENST00000611156.4:c.996C=	ENSP00000483265.1:p.Pro332=
NM_020469.2:c.999C=	NP_065202.2:p.Pro333=
NM_020469.3:c.999C=	NP_065202.2:p.Pro333=