Canonical Allele Identifier: CA479694253

Gene: ARID2

Linked Data

• dbSNP Id: rs2138181865
• MyVariant Identifiers: chr12:g.46246628T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852845T>G , CM000674.2:g.45852845T>G	GRCh38
NC_000012.11:g.46246628T>G , CM000674.1:g.46246628T>G	GRCh37
NC_000012.10:g.44532895T>G	NCBI36
NG_052800.1:g.128181T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4722T>G	ENSP00000415650.3:p.Val1574=
ENST00000457135.2:c.931T>G
ENST00000334344.11:c.4722T>G MANE Select	ENSP00000335044.6:p.Val1574=
ENST00000422737.6:c.4643T>G
ENST00000334344.10:c.4722T>G	ENSP00000335044.6:p.Val1574=
ENST00000422737.5:c.4275T>G	ENSP00000415650.1:p.Val1425=
ENST00000444670.5:c.3552T>G	ENSP00000397307.1:p.Val1184=
ENST00000457135.1:c.546T>G	ENSP00000388357.1:p.Val182=
ENST00000479608.5:n.4013T>G
NM_152641.2:c.4722T>G	NP_689854.2:p.Val1574=
XM_006719272.2:c.4722T>G	XP_006719335.1:p.Val1574=
XM_011538025.1:c.3090T>G	XP_011536327.1:p.Val1030=
XR_944505.1:n.4870T>G
NM_001347839.1:c.4722T>G	NP_001334768.1:p.Val1574=
NM_152641.3:c.4722T>G	NP_689854.2:p.Val1574=
XM_006719272.4:c.4722T>G	XP_006719335.1:p.Val1574=
XR_944505.3:n.4853T>G
NM_152641.4:c.4722T>G MANE Select	NP_689854.2:p.Val1574=
NM_001347839.2:c.4722T>G	NP_001334768.1:p.Val1574=