Canonical Allele Identifier: CA1882581975

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257035G= , CM000671.2:g.133257035G=	GRCh38
NC_000009.11:g.136132422G= , CM000671.1:g.136132422G=	GRCh37
NC_000009.10:g.135122243G=	NCBI36
NG_006669.1:g.20633C=
NG_006669.2:g.23181C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.403+374C=
ENST00000647353.1:n.54-5883C=
ENST00000651471.1:n.330-679C=
ENST00000679909.1:c.28+18127C=	ENSP00000506089.1:n.28+18127C=
ENST00000453660.3:n.385+374C=
ENST00000538324.2:c.371+374C=	ENSP00000483018.1:n.371+374C=
ENST00000611156.4:c.371+374C=	ENSP00000483265.1:n.371+374C=
NM_020469.2:c.374+374C=	NP_065202.2:n.374+374C=
NM_020469.3:c.374+374C=	NP_065202.2:n.374+374C=