Canonical Allele Identifier: CA467852869

Gene: ABO

Linked Data

• gnomAD v4: 9-133256026-G-A
• MyVariant Identifiers: chr9:g.136131413G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256026G>A , CM000671.2:g.133256026G>A	GRCh38
NC_000009.11:g.136131413G>A , CM000671.1:g.136131413G>A	GRCh37
NC_000009.10:g.135121234G>A	NCBI36
NG_006669.1:g.21642C>T
NG_006669.2:g.24190C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.734C>T
ENST00000647353.1:n.54-4874C>T
ENST00000679909.1:c.28+19136C>T	ENSP00000506089.1:n.28+19136C>T
ENST00000453660.3:n.716C>T
ENST00000538324.2:c.702C>T	ENSP00000483018.1:p.Gly234=
ENST00000611156.4:c.702C>T	ENSP00000483265.1:p.Gly234=
NM_020469.2:c.705C>T	NP_065202.2:p.Gly235=
NM_020469.3:c.705C>T	NP_065202.2:p.Gly235=