Canonical Allele Identifier: CA384492177

Gene: ARID2

Linked Data

• dbSNP Id: rs1161560614
• gnomAD v3: 12-45852774-G-A
• gnomAD v4: 12-45852774-G-A
• COSMIC: COSM268370
• MyVariant Identifiers: chr12:g.46246557G>A (hg19) ; chr12:g.45852774G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852774G>A , CM000674.2:g.45852774G>A	GRCh38
NC_000012.11:g.46246557G>A , CM000674.1:g.46246557G>A	GRCh37
NC_000012.10:g.44532824G>A	NCBI36
NG_052800.1:g.128110G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4651G>A	ENSP00000415650.3:p.Ala1551Thr
ENST00000457135.2:c.860G>A
ENST00000334344.11:c.4651G>A MANE Select	ENSP00000335044.6:p.Ala1551Thr
ENST00000422737.6:c.4572G>A
ENST00000334344.10:c.4651G>A	ENSP00000335044.6:p.Ala1551Thr
ENST00000422737.5:c.4204G>A	ENSP00000415650.1:p.Ala1402Thr
ENST00000444670.5:c.3481G>A	ENSP00000397307.1:p.Ala1161Thr
ENST00000457135.1:c.475G>A	ENSP00000388357.1:p.Ala159Thr
ENST00000479608.5:n.3942G>A
NM_152641.2:c.4651G>A	NP_689854.2:p.Ala1551Thr
XM_006719272.2:c.4651G>A	XP_006719335.1:p.Ala1551Thr
XM_011538025.1:c.3019G>A	XP_011536327.1:p.Ala1007Thr
XR_944505.1:n.4799G>A
NM_001347839.1:c.4651G>A	NP_001334768.1:p.Ala1551Thr
NM_152641.3:c.4651G>A	NP_689854.2:p.Ala1551Thr
XM_006719272.4:c.4651G>A	XP_006719335.1:p.Ala1551Thr
XR_944505.3:n.4782G>A
NM_152641.4:c.4651G>A MANE Select	NP_689854.2:p.Ala1551Thr
NM_001347839.2:c.4651G>A	NP_001334768.1:p.Ala1551Thr