Canonical Allele Identifier: CA467852831

Gene: ABO

Linked Data

• gnomAD v4: 9-133256008-C-T
• MyVariant Identifiers: chr9:g.136131395C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256008C>T , CM000671.2:g.133256008C>T	GRCh38
NC_000009.11:g.136131395C>T , CM000671.1:g.136131395C>T	GRCh37
NC_000009.10:g.135121216C>T	NCBI36
NG_006669.1:g.21660G>A
NG_006669.2:g.24208G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.752G>A
ENST00000647353.1:n.54-4856G>A
ENST00000679909.1:c.28+19154G>A	ENSP00000506089.1:n.28+19154G>A
ENST00000453660.3:n.734G>A
ENST00000538324.2:c.720G>A	ENSP00000483018.1:p.Arg240=
ENST00000611156.4:c.720G>A	ENSP00000483265.1:p.Arg240=
NM_020469.2:c.723G>A	NP_065202.2:p.Arg241=
NM_020469.3:c.723G>A	NP_065202.2:p.Arg241=