Canonical Allele Identifier: CA467853017

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131488C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256101C>G , CM000671.2:g.133256101C>G	GRCh38
NC_000009.11:g.136131488C>G , CM000671.1:g.136131488C>G	GRCh37
NC_000009.10:g.135121309C>G	NCBI36
NG_006669.1:g.21567G>C
NG_006669.2:g.24115G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.659G>C
ENST00000647353.1:n.54-4949G>C
ENST00000679909.1:c.28+19061G>C	ENSP00000506089.1:n.28+19061G>C
ENST00000453660.3:n.641G>C
ENST00000538324.2:c.627G>C	ENSP00000483018.1:p.Val209=
ENST00000611156.4:c.627G>C	ENSP00000483265.1:p.Val209=
NM_020469.2:c.630G>C	NP_065202.2:p.Val210=
NM_020469.3:c.630G>C	NP_065202.2:p.Val210=