Canonical Allele Identifier: CA384492129

Gene: ARID2

Linked Data

• dbSNP Id: rs2138181108
• MyVariant Identifiers: chr12:g.46246535C>G (hg19) ; chr12:g.45852752C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852752C>G , CM000674.2:g.45852752C>G	GRCh38
NC_000012.11:g.46246535C>G , CM000674.1:g.46246535C>G	GRCh37
NC_000012.10:g.44532802C>G	NCBI36
NG_052800.1:g.128088C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4629C>G	ENSP00000415650.3:p.Asp1543Glu
ENST00000457135.2:c.838C>G
ENST00000334344.11:c.4629C>G MANE Select	ENSP00000335044.6:p.Asp1543Glu
ENST00000422737.6:c.4550C>G
ENST00000334344.10:c.4629C>G	ENSP00000335044.6:p.Asp1543Glu
ENST00000422737.5:c.4182C>G	ENSP00000415650.1:p.Asp1394Glu
ENST00000444670.5:c.3459C>G	ENSP00000397307.1:p.Asp1153Glu
ENST00000457135.1:c.453C>G	ENSP00000388357.1:p.Asp151Glu
ENST00000479608.5:n.3920C>G
NM_152641.2:c.4629C>G	NP_689854.2:p.Asp1543Glu
XM_006719272.2:c.4629C>G	XP_006719335.1:p.Asp1543Glu
XM_011538025.1:c.2997C>G	XP_011536327.1:p.Asp999Glu
XR_944505.1:n.4777C>G
NM_001347839.1:c.4629C>G	NP_001334768.1:p.Asp1543Glu
NM_152641.3:c.4629C>G	NP_689854.2:p.Asp1543Glu
XM_006719272.4:c.4629C>G	XP_006719335.1:p.Asp1543Glu
XR_944505.3:n.4760C>G
NM_152641.4:c.4629C>G MANE Select	NP_689854.2:p.Asp1543Glu
NM_001347839.2:c.4629C>G	NP_001334768.1:p.Asp1543Glu