Canonical Allele Identifier: CA1882580712

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256233G= , CM000671.2:g.133256233G=	GRCh38
NC_000009.11:g.136131620G= , CM000671.1:g.136131620G=	GRCh37
NC_000009.10:g.135121441G=	NCBI36
NG_006669.1:g.21435C=
NG_006669.2:g.23983C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.527C=
ENST00000647353.1:n.54-5081C=
ENST00000651471.1:n.453C=
ENST00000679909.1:c.28+18929C=	ENSP00000506089.1:n.28+18929C=
ENST00000453660.3:n.509C=
ENST00000538324.2:c.495C=	ENSP00000483018.1:p.Thr165=
ENST00000611156.4:c.495C=	ENSP00000483265.1:p.Thr165=
NM_020469.2:c.498C=	NP_065202.2:p.Thr166=
NM_020469.3:c.498C=	NP_065202.2:p.Thr166=