Canonical Allele Identifier: CA1882580281

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256075T= , CM000671.2:g.133256075T=	GRCh38
NC_000009.11:g.136131462T= , CM000671.1:g.136131462T=	GRCh37
NC_000009.10:g.135121283T=	NCBI36
NG_006669.1:g.21593A=
NG_006669.2:g.24141A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.685A=
ENST00000647353.1:n.54-4923A=
ENST00000679909.1:c.28+19087A=	ENSP00000506089.1:n.28+19087A=
ENST00000453660.3:n.667A=
ENST00000538324.2:c.653A=	ENSP00000483018.1:p.His218=
ENST00000611156.4:c.653A=	ENSP00000483265.1:p.His218=
NM_020469.2:c.656A=	NP_065202.2:p.His219=
NM_020469.3:c.656A=	NP_065202.2:p.His219=