Canonical Allele Identifier: CA1882580921

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256312T= , CM000671.2:g.133256312T=	GRCh38
NC_000009.11:g.136131699T= , CM000671.1:g.136131699T=	GRCh37
NC_000009.10:g.135121520T=	NCBI36
NG_006669.1:g.21356A=
NG_006669.2:g.23904A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.448A=
ENST00000647353.1:n.54-5160A=
ENST00000651471.1:n.374A=
ENST00000679909.1:c.28+18850A=	ENSP00000506089.1:n.28+18850A=
ENST00000453660.3:n.430A=
ENST00000538324.2:c.416A=	ENSP00000483018.1:p.His139=
ENST00000611156.4:c.416A=	ENSP00000483265.1:p.His139=
NM_020469.2:c.419A=	NP_065202.2:p.His140=
NM_020469.3:c.419A=	NP_065202.2:p.His140=