Canonical Allele Identifier: CA384491230

Gene: ARID2

Linked Data

• dbSNP Id: rs2138179061
• MyVariant Identifiers: chr12:g.46246254G>C (hg19) ; chr12:g.45852471G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852471G>C , CM000674.2:g.45852471G>C	GRCh38
NC_000012.11:g.46246254G>C , CM000674.1:g.46246254G>C	GRCh37
NC_000012.10:g.44532521G>C	NCBI36
NG_052800.1:g.127807G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4348G>C	ENSP00000415650.3:p.Gly1450Arg
ENST00000457135.2:c.557G>C
ENST00000334344.11:c.4348G>C MANE Select	ENSP00000335044.6:p.Gly1450Arg
ENST00000422737.6:c.4269G>C
ENST00000334344.10:c.4348G>C	ENSP00000335044.6:p.Gly1450Arg
ENST00000422737.5:c.3901G>C	ENSP00000415650.1:p.Gly1301Arg
ENST00000444670.5:c.3178G>C	ENSP00000397307.1:p.Gly1060Arg
ENST00000457135.1:c.172G>C	ENSP00000388357.1:p.Gly58Arg
ENST00000479608.5:n.3639G>C
NM_152641.2:c.4348G>C	NP_689854.2:p.Gly1450Arg
XM_006719272.2:c.4348G>C	XP_006719335.1:p.Gly1450Arg
XM_011538025.1:c.2716G>C	XP_011536327.1:p.Gly906Arg
XR_944505.1:n.4496G>C
NM_001347839.1:c.4348G>C	NP_001334768.1:p.Gly1450Arg
NM_152641.3:c.4348G>C	NP_689854.2:p.Gly1450Arg
XM_006719272.4:c.4348G>C	XP_006719335.1:p.Gly1450Arg
XR_944505.3:n.4479G>C
NM_152641.4:c.4348G>C MANE Select	NP_689854.2:p.Gly1450Arg
NM_001347839.2:c.4348G>C	NP_001334768.1:p.Gly1450Arg