Canonical Allele Identifier: CA1882581048

Gene: ABO

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256372A= , CM000671.2:g.133256372A=	GRCh38
NC_000009.11:g.136131759A= , CM000671.1:g.136131759A=	GRCh37
NC_000009.10:g.135121580A=	NCBI36
NG_006669.1:g.21296T=
NG_006669.2:g.23844T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.404-16T=
ENST00000647353.1:n.54-5220T=
ENST00000651471.1:n.330-16T=
ENST00000679909.1:c.28+18790T=	ENSP00000506089.1:n.28+18790T=
ENST00000453660.3:n.386-16T=
ENST00000538324.2:c.372-16T=	ENSP00000483018.1:n.372-16T=
ENST00000611156.4:c.372-16T=	ENSP00000483265.1:n.372-16T=
NM_020469.2:c.375-16T=	NP_065202.2:n.375-16T=
NM_020469.3:c.375-16T=	NP_065202.2:n.375-16T=