Canonical Allele Identifier: CA384491850

Gene: ARID2

Linked Data

• dbSNP Id: rs1324779117
• MyVariant Identifiers: chr12:g.46246402T>A (hg19) ; chr12:g.45852619T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852619T>A , CM000674.2:g.45852619T>A	GRCh38
NC_000012.11:g.46246402T>A , CM000674.1:g.46246402T>A	GRCh37
NC_000012.10:g.44532669T>A	NCBI36
NG_052800.1:g.127955T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4496T>A	ENSP00000415650.3:p.Leu1499Gln
ENST00000457135.2:c.705T>A
ENST00000334344.11:c.4496T>A MANE Select	ENSP00000335044.6:p.Leu1499Gln
ENST00000422737.6:c.4417T>A
ENST00000334344.10:c.4496T>A	ENSP00000335044.6:p.Leu1499Gln
ENST00000422737.5:c.4049T>A	ENSP00000415650.1:p.Leu1350Gln
ENST00000444670.5:c.3326T>A	ENSP00000397307.1:p.Leu1109Gln
ENST00000457135.1:c.320T>A	ENSP00000388357.1:p.Leu107Gln
ENST00000479608.5:n.3787T>A
NM_152641.2:c.4496T>A	NP_689854.2:p.Leu1499Gln
XM_006719272.2:c.4496T>A	XP_006719335.1:p.Leu1499Gln
XM_011538025.1:c.2864T>A	XP_011536327.1:p.Leu955Gln
XR_944505.1:n.4644T>A
NM_001347839.1:c.4496T>A	NP_001334768.1:p.Leu1499Gln
NM_152641.3:c.4496T>A	NP_689854.2:p.Leu1499Gln
XM_006719272.4:c.4496T>A	XP_006719335.1:p.Leu1499Gln
XR_944505.3:n.4627T>A
NM_152641.4:c.4496T>A MANE Select	NP_689854.2:p.Leu1499Gln
NM_001347839.2:c.4496T>A	NP_001334768.1:p.Leu1499Gln