Canonical Allele Identifier: CA384492154
Gene: ARID2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3129426
ClinVar RCV Id: RCV004425292
dbSNP Id: rs1943579927

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852763C>T , CM000674.2:g.45852763C>T GRCh38
NC_000012.11:g.46246546C>T , CM000674.1:g.46246546C>T GRCh37
NC_000012.10:g.44532813C>T NCBI36
NG_052800.1:g.128099C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4640C>T ENSP00000415650.3:p.Ala1547Val
ENST00000457135.2:c.849C>T
ENST00000334344.11:c.4640C>T MANE Select ENSP00000335044.6:p.Ala1547Val
ENST00000422737.6:c.4561C>T
ENST00000334344.10:c.4640C>T ENSP00000335044.6:p.Ala1547Val
ENST00000422737.5:c.4193C>T ENSP00000415650.1:p.Ala1398Val
ENST00000444670.5:c.3470C>T ENSP00000397307.1:p.Ala1157Val
ENST00000457135.1:c.464C>T ENSP00000388357.1:p.Ala155Val
ENST00000479608.5:n.3931C>T
NM_152641.2:c.4640C>T NP_689854.2:p.Ala1547Val
XM_006719272.2:c.4640C>T XP_006719335.1:p.Ala1547Val
XM_011538025.1:c.3008C>T XP_011536327.1:p.Ala1003Val
XR_944505.1:n.4788C>T
NM_001347839.1:c.4640C>T NP_001334768.1:p.Ala1547Val
NM_152641.3:c.4640C>T NP_689854.2:p.Ala1547Val
XM_006719272.4:c.4640C>T XP_006719335.1:p.Ala1547Val
XR_944505.3:n.4771C>T
NM_152641.4:c.4640C>T MANE Select NP_689854.2:p.Ala1547Val
NM_001347839.2:c.4640C>T NP_001334768.1:p.Ala1547Val