Canonical Allele Identifier: CA467853043

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131272C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255885C>T , CM000671.2:g.133255885C>T	GRCh38
NC_000009.11:g.136131272C>T , CM000671.1:g.136131272C>T	GRCh37
NC_000009.10:g.135121093C>T	NCBI36
NG_006669.1:g.21783G>A
NG_006669.2:g.24331G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.875G>A
ENST00000647353.1:n.54-4733G>A
ENST00000679909.1:c.28+19277G>A	ENSP00000506089.1:n.28+19277G>A
ENST00000453660.3:n.857G>A
ENST00000538324.2:c.843G>A	ENSP00000483018.1:p.Arg281=
ENST00000611156.4:c.843G>A	ENSP00000483265.1:p.Arg281=
NM_020469.2:c.846G>A	NP_065202.2:p.Arg282=
NM_020469.3:c.846G>A	NP_065202.2:p.Arg282=