Canonical Allele Identifier: CA384491908

Gene: ARID2

Linked Data

• dbSNP Id: rs1184036990
• MyVariant Identifiers: chr12:g.46246432C>G (hg19) ; chr12:g.45852649C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852649C>G , CM000674.2:g.45852649C>G	GRCh38
NC_000012.11:g.46246432C>G , CM000674.1:g.46246432C>G	GRCh37
NC_000012.10:g.44532699C>G	NCBI36
NG_052800.1:g.127985C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4526C>G	ENSP00000415650.3:p.Thr1509Arg
ENST00000457135.2:c.735C>G
ENST00000334344.11:c.4526C>G MANE Select	ENSP00000335044.6:p.Thr1509Arg
ENST00000422737.6:c.4447C>G
ENST00000334344.10:c.4526C>G	ENSP00000335044.6:p.Thr1509Arg
ENST00000422737.5:c.4079C>G	ENSP00000415650.1:p.Thr1360Arg
ENST00000444670.5:c.3356C>G	ENSP00000397307.1:p.Thr1119Arg
ENST00000457135.1:c.350C>G	ENSP00000388357.1:p.Thr117Arg
ENST00000479608.5:n.3817C>G
NM_152641.2:c.4526C>G	NP_689854.2:p.Thr1509Arg
XM_006719272.2:c.4526C>G	XP_006719335.1:p.Thr1509Arg
XM_011538025.1:c.2894C>G	XP_011536327.1:p.Thr965Arg
XR_944505.1:n.4674C>G
NM_001347839.1:c.4526C>G	NP_001334768.1:p.Thr1509Arg
NM_152641.3:c.4526C>G	NP_689854.2:p.Thr1509Arg
XM_006719272.4:c.4526C>G	XP_006719335.1:p.Thr1509Arg
XR_944505.3:n.4657C>G
NM_152641.4:c.4526C>G MANE Select	NP_689854.2:p.Thr1509Arg
NM_001347839.2:c.4526C>G	NP_001334768.1:p.Thr1509Arg