Canonical Allele Identifier: CA1882590556

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274133C= , CM000671.2:g.133274133C=	GRCh38
NC_000009.11:g.136149549C= , CM000671.1:g.136149549C=	GRCh37
NC_000009.10:g.135139370C=	NCBI36
NG_006669.1:g.3502G=
NG_006669.2:g.6082G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.58+1029G=
ENST00000647353.1:n.53+1029G=
ENST00000651471.1:n.63+1829G=
ENST00000679909.1:c.28+1029G=	ENSP00000506089.1:n.28+1029G=
ENST00000453660.3:n.40+1029G=
ENST00000538324.2:c.28+1029G=	ENSP00000483018.1:n.28+1029G=
ENST00000611156.4:c.28+1029G=	ENSP00000483265.1:n.28+1029G=
NM_020469.2:c.28+1029G=	NP_065202.2:n.28+1029G=
NM_020469.3:c.28+1029G=	NP_065202.2:n.28+1029G=