Canonical Allele Identifier: CA1882582984

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258053C= , CM000671.2:g.133258053C=	GRCh38
NC_000009.11:g.136133443C= , CM000671.1:g.136133443C=	GRCh37
NC_000009.10:g.135123264C=	NCBI36
NG_006669.1:g.19611G=
NG_006669.2:g.22162G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.269+44G=
ENST00000647353.1:n.54-6901G=
ENST00000651471.1:n.318G=
ENST00000679909.1:c.28+17109G=	ENSP00000506089.1:n.28+17109G=
ENST00000453660.3:n.251+44G=
ENST00000538324.2:c.239+44G=	ENSP00000483018.1:n.239+44G=
ENST00000611156.4:c.239+44G=	ENSP00000483265.1:n.239+44G=
NM_020469.2:c.239+44G=	NP_065202.2:n.239+44G=
NM_020469.3:c.239+44G=	NP_065202.2:n.239+44G=