Canonical Allele Identifier: CA479694110

Gene: ARID2

Linked Data

• MyVariant Identifiers: chr12:g.46246493A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852710A>T , CM000674.2:g.45852710A>T	GRCh38
NC_000012.11:g.46246493A>T , CM000674.1:g.46246493A>T	GRCh37
NC_000012.10:g.44532760A>T	NCBI36
NG_052800.1:g.128046A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4587A>T	ENSP00000415650.3:p.Gly1529=
ENST00000457135.2:c.796A>T
ENST00000334344.11:c.4587A>T MANE Select	ENSP00000335044.6:p.Gly1529=
ENST00000422737.6:c.4508A>T
ENST00000334344.10:c.4587A>T	ENSP00000335044.6:p.Gly1529=
ENST00000422737.5:c.4140A>T	ENSP00000415650.1:p.Gly1380=
ENST00000444670.5:c.3417A>T	ENSP00000397307.1:p.Gly1139=
ENST00000457135.1:c.411A>T	ENSP00000388357.1:p.Gly137=
ENST00000479608.5:n.3878A>T
NM_152641.2:c.4587A>T	NP_689854.2:p.Gly1529=
XM_006719272.2:c.4587A>T	XP_006719335.1:p.Gly1529=
XM_011538025.1:c.2955A>T	XP_011536327.1:p.Gly985=
XR_944505.1:n.4735A>T
NM_001347839.1:c.4587A>T	NP_001334768.1:p.Gly1529=
NM_152641.3:c.4587A>T	NP_689854.2:p.Gly1529=
XM_006719272.4:c.4587A>T	XP_006719335.1:p.Gly1529=
XR_944505.3:n.4718A>T
NM_152641.4:c.4587A>T MANE Select	NP_689854.2:p.Gly1529=
NM_001347839.2:c.4587A>T	NP_001334768.1:p.Gly1529=