Canonical Allele Identifier: CA156944

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45839470C>G , CM000674.2:g.45839470C>G	GRCh38
NC_000012.11:g.46233253C>G , CM000674.1:g.46233253C>G	GRCh37
NC_000012.10:g.44519520C>G	NCBI36
NG_052800.1:g.114806C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.1472C>G	ENSP00000415650.3:p.Thr491Ser
ENST00000334344.11:c.1472C>G MANE Select	ENSP00000335044.6:p.Thr491Ser
ENST00000422737.6:c.1393C>G
ENST00000334344.10:c.1472C>G	ENSP00000335044.6:p.Thr491Ser
ENST00000422737.5:c.1025C>G	ENSP00000415650.1:p.Thr342Ser
ENST00000444670.5:c.302C>G	ENSP00000397307.1:p.Thr101Ser
ENST00000479608.5:n.680C>G
ENST00000480128.1:n.496C>G
NM_152641.2:c.1472C>G	NP_689854.2:p.Thr491Ser
XM_006719272.2:c.1472C>G	XP_006719335.1:p.Thr491Ser
XM_011538025.1:c.-244C>G	XP_011536327.1:n.-244C>G
XR_944505.1:n.1620C>G
XR_944892.1:n.289+382G>C
XR_944893.1:n.289+382G>C
NM_001347839.1:c.1472C>G	NP_001334768.1:p.Thr491Ser
NM_152641.3:c.1472C>G	NP_689854.2:p.Thr491Ser
XM_006719272.4:c.1472C>G	XP_006719335.1:p.Thr491Ser
XR_001749098.1:n.476+382G>C
XR_944505.3:n.1603C>G
XR_944892.2:n.289+382G>C
NM_152641.4:c.1472C>G MANE Select	NP_689854.2:p.Thr491Ser
NM_001347839.2:c.1472C>G	NP_001334768.1:p.Thr491Ser