Canonical Allele Identifier: CA467853095

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131302C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255915C>G , CM000671.2:g.133255915C>G	GRCh38
NC_000009.11:g.136131302C>G , CM000671.1:g.136131302C>G	GRCh37
NC_000009.10:g.135121123C>G	NCBI36
NG_006669.1:g.21753G>C
NG_006669.2:g.24301G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.845G>C
ENST00000647353.1:n.54-4763G>C
ENST00000679909.1:c.28+19247G>C	ENSP00000506089.1:n.28+19247G>C
ENST00000453660.3:n.827G>C
ENST00000538324.2:c.813G>C	ENSP00000483018.1:p.Gly271=
ENST00000611156.4:c.813G>C	ENSP00000483265.1:p.Gly271=
NM_020469.2:c.816G>C	NP_065202.2:p.Gly272=
NM_020469.3:c.816G>C	NP_065202.2:p.Gly272=