Canonical Allele Identifier: CA479694181

Gene: ARID2

Linked Data

• MyVariant Identifiers: chr12:g.46246574G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852791G>C , CM000674.2:g.45852791G>C	GRCh38
NC_000012.11:g.46246574G>C , CM000674.1:g.46246574G>C	GRCh37
NC_000012.10:g.44532841G>C	NCBI36
NG_052800.1:g.128127G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4668G>C	ENSP00000415650.3:p.Val1556=
ENST00000457135.2:c.877G>C
ENST00000334344.11:c.4668G>C MANE Select	ENSP00000335044.6:p.Val1556=
ENST00000422737.6:c.4589G>C
ENST00000334344.10:c.4668G>C	ENSP00000335044.6:p.Val1556=
ENST00000422737.5:c.4221G>C	ENSP00000415650.1:p.Val1407=
ENST00000444670.5:c.3498G>C	ENSP00000397307.1:p.Val1166=
ENST00000457135.1:c.492G>C	ENSP00000388357.1:p.Val164=
ENST00000479608.5:n.3959G>C
NM_152641.2:c.4668G>C	NP_689854.2:p.Val1556=
XM_006719272.2:c.4668G>C	XP_006719335.1:p.Val1556=
XM_011538025.1:c.3036G>C	XP_011536327.1:p.Val1012=
XR_944505.1:n.4816G>C
NM_001347839.1:c.4668G>C	NP_001334768.1:p.Val1556=
NM_152641.3:c.4668G>C	NP_689854.2:p.Val1556=
XM_006719272.4:c.4668G>C	XP_006719335.1:p.Val1556=
XR_944505.3:n.4799G>C
NM_152641.4:c.4668G>C MANE Select	NP_689854.2:p.Val1556=
NM_001347839.2:c.4668G>C	NP_001334768.1:p.Val1556=