Canonical Allele Identifier: CA384452476
Gene: ARID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45904949T>A , CM000674.2:g.45904949T>A GRCh38
NC_000012.11:g.46298732T>A , CM000674.1:g.46298732T>A GRCh37
NC_000012.10:g.44584999T>A NCBI36
NG_052800.1:g.180285T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000457135.2:c.1645T>A
ENST00000334344.11:c.5379T>A MANE Select ENSP00000335044.6:p.His1793Gln
ENST00000334344.10:c.5379T>A ENSP00000335044.6:p.His1793Gln
ENST00000444670.5:c.4209T>A ENSP00000397307.1:p.His1403Gln
ENST00000457135.1:c.*54T>A ENSP00000388357.1:n.*54T>A
ENST00000479608.5:n.4670T>A
NM_152641.2:c.5379T>A NP_689854.2:p.His1793Gln
XM_006719272.2:c.*54T>A XP_006719335.1:n.*54T>A
XM_011538025.1:c.3747T>A XP_011536327.1:p.His1249Gln
XR_944505.1:n.5585T>A
NM_152641.3:c.5379T>A NP_689854.2:p.His1793Gln
XM_006719272.4:c.*54T>A XP_006719335.1:n.*54T>A
XR_944505.3:n.5568T>A
NM_152641.4:c.5379T>A MANE Select NP_689854.2:p.His1793Gln