Canonical Allele Identifier: CA6526705
Gene: ARID2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2429828
ClinVar RCV Id: RCV003127267
dbSNP Id: rs138175128

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852816G>A , CM000674.2:g.45852816G>A GRCh38
NC_000012.11:g.46246599G>A , CM000674.1:g.46246599G>A GRCh37
NC_000012.10:g.44532866G>A NCBI36
NG_052800.1:g.128152G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4693G>A ENSP00000415650.3:p.Val1565Ile
ENST00000457135.2:c.902G>A
ENST00000334344.11:c.4693G>A MANE Select ENSP00000335044.6:p.Val1565Ile
ENST00000422737.6:c.4614G>A
ENST00000334344.10:c.4693G>A ENSP00000335044.6:p.Val1565Ile
ENST00000422737.5:c.4246G>A ENSP00000415650.1:p.Val1416Ile
ENST00000444670.5:c.3523G>A ENSP00000397307.1:p.Val1175Ile
ENST00000457135.1:c.517G>A ENSP00000388357.1:p.Val173Ile
ENST00000479608.5:n.3984G>A
NM_152641.2:c.4693G>A NP_689854.2:p.Val1565Ile
XM_006719272.2:c.4693G>A XP_006719335.1:p.Val1565Ile
XM_011538025.1:c.3061G>A XP_011536327.1:p.Val1021Ile
XR_944505.1:n.4841G>A
NM_001347839.1:c.4693G>A NP_001334768.1:p.Val1565Ile
NM_152641.3:c.4693G>A NP_689854.2:p.Val1565Ile
XM_006719272.4:c.4693G>A XP_006719335.1:p.Val1565Ile
XR_944505.3:n.4824G>A
NM_152641.4:c.4693G>A MANE Select NP_689854.2:p.Val1565Ile
NM_001347839.2:c.4693G>A NP_001334768.1:p.Val1565Ile