Canonical Allele Identifier: CA384492159
Gene: ARID2 HGNC NCBI

Linked Data

dbSNP Id: rs1297331867

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852766G>A , CM000674.2:g.45852766G>A GRCh38
NC_000012.11:g.46246549G>A , CM000674.1:g.46246549G>A GRCh37
NC_000012.10:g.44532816G>A NCBI36
NG_052800.1:g.128102G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4643G>A ENSP00000415650.3:p.Gly1548Asp
ENST00000457135.2:c.852G>A
ENST00000334344.11:c.4643G>A MANE Select ENSP00000335044.6:p.Gly1548Asp
ENST00000422737.6:c.4564G>A
ENST00000334344.10:c.4643G>A ENSP00000335044.6:p.Gly1548Asp
ENST00000422737.5:c.4196G>A ENSP00000415650.1:p.Gly1399Asp
ENST00000444670.5:c.3473G>A ENSP00000397307.1:p.Gly1158Asp
ENST00000457135.1:c.467G>A ENSP00000388357.1:p.Gly156Asp
ENST00000479608.5:n.3934G>A
NM_152641.2:c.4643G>A NP_689854.2:p.Gly1548Asp
XM_006719272.2:c.4643G>A XP_006719335.1:p.Gly1548Asp
XM_011538025.1:c.3011G>A XP_011536327.1:p.Gly1004Asp
XR_944505.1:n.4791G>A
NM_001347839.1:c.4643G>A NP_001334768.1:p.Gly1548Asp
NM_152641.3:c.4643G>A NP_689854.2:p.Gly1548Asp
XM_006719272.4:c.4643G>A XP_006719335.1:p.Gly1548Asp
XR_944505.3:n.4774G>A
NM_152641.4:c.4643G>A MANE Select NP_689854.2:p.Gly1548Asp
NM_001347839.2:c.4643G>A NP_001334768.1:p.Gly1548Asp