Canonical Allele Identifier: CA467853016

Gene: ABO

Linked Data

• gnomAD v4: 9-133256101-C-T
• MyVariant Identifiers: chr9:g.136131488C>T (hg19)

Genomic Alleles

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

Transcript Alleles

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