Canonical Allele Identifier: CA1882580230

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256038G= , CM000671.2:g.133256038G=	GRCh38
NC_000009.11:g.136131425G= , CM000671.1:g.136131425G=	GRCh37
NC_000009.10:g.135121246G=	NCBI36
NG_006669.1:g.21630C=
NG_006669.2:g.24178C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.722C=
ENST00000647353.1:n.54-4886C=
ENST00000679909.1:c.28+19124C=	ENSP00000506089.1:n.28+19124C=
ENST00000453660.3:n.704C=
ENST00000538324.2:c.690C=	ENSP00000483018.1:p.Thr230=
ENST00000611156.4:c.690C=	ENSP00000483265.1:p.Thr230=
NM_020469.2:c.693C=	NP_065202.2:p.Thr231=
NM_020469.3:c.693C=	NP_065202.2:p.Thr231=