Canonical Allele Identifier: CA2033475691
Gene: ARID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852597A= , CM000674.2:g.45852597A= GRCh38
NC_000012.11:g.46246380A= , CM000674.1:g.46246380A= GRCh37
NC_000012.10:g.44532647A= NCBI36
NG_052800.1:g.127933A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4474A= ENSP00000415650.3:p.Lys1492=
ENST00000457135.2:c.683A=
ENST00000334344.11:c.4474A= MANE Select ENSP00000335044.6:p.Lys1492=
ENST00000422737.6:c.4395A=
ENST00000334344.10:c.4474A= ENSP00000335044.6:p.Lys1492=
ENST00000422737.5:c.4027A= ENSP00000415650.1:p.Lys1343=
ENST00000444670.5:c.3304A= ENSP00000397307.1:p.Lys1102=
ENST00000457135.1:c.298A= ENSP00000388357.1:p.Lys100=
ENST00000479608.5:n.3765A=
NM_152641.2:c.4474A= NP_689854.2:p.Lys1492=
XM_006719272.2:c.4474A= XP_006719335.1:p.Lys1492=
XM_011538025.1:c.2842A= XP_011536327.1:p.Lys948=
XR_944505.1:n.4622A=
NM_001347839.1:c.4474A= NP_001334768.1:p.Lys1492=
NM_152641.3:c.4474A= NP_689854.2:p.Lys1492=
XM_006719272.4:c.4474A= XP_006719335.1:p.Lys1492=
XR_944505.3:n.4605A=
NM_152641.4:c.4474A= MANE Select NP_689854.2:p.Lys1492=
NM_001347839.2:c.4474A= NP_001334768.1:p.Lys1492=