Canonical Allele Identifier: CA384492375

Gene: ARID2

Linked Data

• MyVariant Identifiers: chr12:g.46246603C>T (hg19) ; chr12:g.45852820C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852820C>T , CM000674.2:g.45852820C>T	GRCh38
NC_000012.11:g.46246603C>T , CM000674.1:g.46246603C>T	GRCh37
NC_000012.10:g.44532870C>T	NCBI36
NG_052800.1:g.128156C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4697C>T	ENSP00000415650.3:p.Ala1566Val
ENST00000457135.2:c.906C>T
ENST00000334344.11:c.4697C>T MANE Select	ENSP00000335044.6:p.Ala1566Val
ENST00000422737.6:c.4618C>T
ENST00000334344.10:c.4697C>T	ENSP00000335044.6:p.Ala1566Val
ENST00000422737.5:c.4250C>T	ENSP00000415650.1:p.Ala1417Val
ENST00000444670.5:c.3527C>T	ENSP00000397307.1:p.Ala1176Val
ENST00000457135.1:c.521C>T	ENSP00000388357.1:p.Ala174Val
ENST00000479608.5:n.3988C>T
NM_152641.2:c.4697C>T	NP_689854.2:p.Ala1566Val
XM_006719272.2:c.4697C>T	XP_006719335.1:p.Ala1566Val
XM_011538025.1:c.3065C>T	XP_011536327.1:p.Ala1022Val
XR_944505.1:n.4845C>T
NM_001347839.1:c.4697C>T	NP_001334768.1:p.Ala1566Val
NM_152641.3:c.4697C>T	NP_689854.2:p.Ala1566Val
XM_006719272.4:c.4697C>T	XP_006719335.1:p.Ala1566Val
XR_944505.3:n.4828C>T
NM_152641.4:c.4697C>T MANE Select	NP_689854.2:p.Ala1566Val
NM_001347839.2:c.4697C>T	NP_001334768.1:p.Ala1566Val