Canonical Allele Identifier: CA1882582979

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258046A= , CM000671.2:g.133258046A=	GRCh38
NC_000009.11:g.136133436A= , CM000671.1:g.136133436A=	GRCh37
NC_000009.10:g.135123257A=	NCBI36
NG_006669.1:g.19618T=
NG_006669.2:g.22169T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.269+51T=
ENST00000647353.1:n.54-6894T=
ENST00000651471.1:n.325T=
ENST00000679909.1:c.28+17116T=	ENSP00000506089.1:n.28+17116T=
ENST00000453660.3:n.251+51T=
ENST00000538324.2:c.239+51T=	ENSP00000483018.1:n.239+51T=
ENST00000611156.4:c.239+51T=	ENSP00000483265.1:n.239+51T=
NM_020469.2:c.239+51T=	NP_065202.2:n.239+51T=
NM_020469.3:c.239+51T=	NP_065202.2:n.239+51T=