Canonical Allele Identifier: CA384491389

Gene: ARID2

Linked Data

• MyVariant Identifiers: chr12:g.46246283T>G (hg19) ; chr12:g.45852500T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852500T>G , CM000674.2:g.45852500T>G	GRCh38
NC_000012.11:g.46246283T>G , CM000674.1:g.46246283T>G	GRCh37
NC_000012.10:g.44532550T>G	NCBI36
NG_052800.1:g.127836T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4377T>G	ENSP00000415650.3:p.Asp1459Glu
ENST00000457135.2:c.586T>G
ENST00000334344.11:c.4377T>G MANE Select	ENSP00000335044.6:p.Asp1459Glu
ENST00000422737.6:c.4298T>G
ENST00000334344.10:c.4377T>G	ENSP00000335044.6:p.Asp1459Glu
ENST00000422737.5:c.3930T>G	ENSP00000415650.1:p.Asp1310Glu
ENST00000444670.5:c.3207T>G	ENSP00000397307.1:p.Asp1069Glu
ENST00000457135.1:c.201T>G	ENSP00000388357.1:p.Asp67Glu
ENST00000479608.5:n.3668T>G
NM_152641.2:c.4377T>G	NP_689854.2:p.Asp1459Glu
XM_006719272.2:c.4377T>G	XP_006719335.1:p.Asp1459Glu
XM_011538025.1:c.2745T>G	XP_011536327.1:p.Asp915Glu
XR_944505.1:n.4525T>G
NM_001347839.1:c.4377T>G	NP_001334768.1:p.Asp1459Glu
NM_152641.3:c.4377T>G	NP_689854.2:p.Asp1459Glu
XM_006719272.4:c.4377T>G	XP_006719335.1:p.Asp1459Glu
XR_944505.3:n.4508T>G
NM_152641.4:c.4377T>G MANE Select	NP_689854.2:p.Asp1459Glu
NM_001347839.2:c.4377T>G	NP_001334768.1:p.Asp1459Glu