Canonical Allele Identifier: CA1882580689

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256227C= , CM000671.2:g.133256227C=	GRCh38
NC_000009.11:g.136131614C= , CM000671.1:g.136131614C=	GRCh37
NC_000009.10:g.135121435C=	NCBI36
NG_006669.1:g.21441G=
NG_006669.2:g.23989G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.533G=
ENST00000647353.1:n.54-5075G=
ENST00000651471.1:n.459G=
ENST00000679909.1:c.28+18935G=	ENSP00000506089.1:n.28+18935G=
ENST00000453660.3:n.515G=
ENST00000538324.2:c.501G=	ENSP00000483018.1:p.Arg167=
ENST00000611156.4:c.501G=	ENSP00000483265.1:p.Arg167=
NM_020469.2:c.504G=	NP_065202.2:p.Arg168=
NM_020469.3:c.504G=	NP_065202.2:p.Arg168=