Canonical Allele Identifier: CA467779965

Gene: ABO

Linked Data

• dbSNP Id: rs1834544516
• gnomAD v4: 9-133255298-C-A
• MyVariant Identifiers: chr9:g.136130685C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255298C>A , CM000671.2:g.133255298C>A	GRCh38
NC_000009.11:g.136130685C>A , CM000671.1:g.136130685C>A	GRCh37
NC_000009.10:g.135120506C>A	NCBI36
NG_006669.1:g.22370G>T
NG_006669.2:g.24918G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1462G>T
ENST00000647353.1:n.54-4146G>T
ENST00000679909.1:c.28+19864G>T	ENSP00000506089.1:n.28+19864G>T
ENST00000453660.3:n.1444G>T
ENST00000611156.4:c.*368G>T	ENSP00000483265.1:n.*368G>T
NM_020469.2:c.*368G>T	NP_065202.2:n.*368G>T
NM_020469.3:c.*368G>T	NP_065202.2:n.*368G>T