Canonical Allele Identifier: CA1882579517

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255791T= , CM000671.2:g.133255791T=	GRCh38
NC_000009.11:g.136131178T= , CM000671.1:g.136131178T=	GRCh37
NC_000009.10:g.135120999T=	NCBI36
NG_006669.1:g.21877A=
NG_006669.2:g.24425A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.969A=
ENST00000647353.1:n.54-4639A=
ENST00000679909.1:c.28+19371A=	ENSP00000506089.1:n.28+19371A=
ENST00000453660.3:n.951A=
ENST00000538324.2:c.937A=	ENSP00000483018.1:p.Lys313=
ENST00000611156.4:c.937A=	ENSP00000483265.1:p.Lys313=
NM_020469.2:c.940A=	NP_065202.2:p.Lys314=
NM_020469.3:c.940A=	NP_065202.2:p.Lys314=