Canonical Allele Identifier: CA467852769

Gene: ABO

Linked Data

• gnomAD v4: 9-133255969-G-T
• MyVariant Identifiers: chr9:g.136131356G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255969G>T , CM000671.2:g.133255969G>T	GRCh38
NC_000009.11:g.136131356G>T , CM000671.1:g.136131356G>T	GRCh37
NC_000009.10:g.135121177G>T	NCBI36
NG_006669.1:g.21699C>A
NG_006669.2:g.24247C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.791C>A
ENST00000647353.1:n.54-4817C>A
ENST00000679909.1:c.28+19193C>A	ENSP00000506089.1:n.28+19193C>A
ENST00000453660.3:n.773C>A
ENST00000538324.2:c.759C>A	ENSP00000483018.1:p.Ala253=
ENST00000611156.4:c.759C>A	ENSP00000483265.1:p.Ala253=
NM_020469.2:c.762C>A	NP_065202.2:p.Ala254=
NM_020469.3:c.762C>A	NP_065202.2:p.Ala254=