Canonical Allele Identifier: CA479694229

Gene: ARID2

Linked Data

• MyVariant Identifiers: chr12:g.46246613A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852830A>C , CM000674.2:g.45852830A>C	GRCh38
NC_000012.11:g.46246613A>C , CM000674.1:g.46246613A>C	GRCh37
NC_000012.10:g.44532880A>C	NCBI36
NG_052800.1:g.128166A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4707A>C	ENSP00000415650.3:p.Ala1569=
ENST00000457135.2:c.916A>C
ENST00000334344.11:c.4707A>C MANE Select	ENSP00000335044.6:p.Ala1569=
ENST00000422737.6:c.4628A>C
ENST00000334344.10:c.4707A>C	ENSP00000335044.6:p.Ala1569=
ENST00000422737.5:c.4260A>C	ENSP00000415650.1:p.Ala1420=
ENST00000444670.5:c.3537A>C	ENSP00000397307.1:p.Ala1179=
ENST00000457135.1:c.531A>C	ENSP00000388357.1:p.Ala177=
ENST00000479608.5:n.3998A>C
NM_152641.2:c.4707A>C	NP_689854.2:p.Ala1569=
XM_006719272.2:c.4707A>C	XP_006719335.1:p.Ala1569=
XM_011538025.1:c.3075A>C	XP_011536327.1:p.Ala1025=
XR_944505.1:n.4855A>C
NM_001347839.1:c.4707A>C	NP_001334768.1:p.Ala1569=
NM_152641.3:c.4707A>C	NP_689854.2:p.Ala1569=
XM_006719272.4:c.4707A>C	XP_006719335.1:p.Ala1569=
XR_944505.3:n.4838A>C
NM_152641.4:c.4707A>C MANE Select	NP_689854.2:p.Ala1569=
NM_001347839.2:c.4707A>C	NP_001334768.1:p.Ala1569=