Canonical Allele Identifier: CA1882579863

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255920C= , CM000671.2:g.133255920C=	GRCh38
NC_000009.11:g.136131307C= , CM000671.1:g.136131307C=	GRCh37
NC_000009.10:g.135121128C=	NCBI36
NG_006669.1:g.21748G=
NG_006669.2:g.24296G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.840G=
ENST00000647353.1:n.54-4768G=
ENST00000679909.1:c.28+19242G=	ENSP00000506089.1:n.28+19242G=
ENST00000453660.3:n.822G=
ENST00000538324.2:c.808G=	ENSP00000483018.1:p.Gly270=
ENST00000611156.4:c.808G=	ENSP00000483265.1:p.Gly270=
NM_020469.2:c.811G=	NP_065202.2:p.Gly271=
NM_020469.3:c.811G=	NP_065202.2:p.Gly271=