Canonical Allele Identifier: CA1882590707

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274453G= , CM000671.2:g.133274453G=	GRCh38
NC_000009.11:g.136149869G= , CM000671.1:g.136149869G=	GRCh37
NC_000009.10:g.135139690G=	NCBI36
NG_006669.1:g.3181C=
NG_006669.2:g.5762C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.58+709C=
ENST00000647353.1:n.53+709C=
ENST00000651471.1:n.63+1509C=
ENST00000679909.1:c.28+709C=	ENSP00000506089.1:n.28+709C=
ENST00000453660.3:n.40+709C=
ENST00000538324.2:c.28+709C=	ENSP00000483018.1:n.28+709C=
ENST00000611156.4:c.28+709C=	ENSP00000483265.1:n.28+709C=
NM_020469.2:c.28+709C=	NP_065202.2:n.28+709C=
NM_020469.3:c.28+709C=	NP_065202.2:n.28+709C=