Canonical Allele Identifier: CA479694217

Gene: ARID2

Linked Data

• MyVariant Identifiers: chr12:g.46246604T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852821T>A , CM000674.2:g.45852821T>A	GRCh38
NC_000012.11:g.46246604T>A , CM000674.1:g.46246604T>A	GRCh37
NC_000012.10:g.44532871T>A	NCBI36
NG_052800.1:g.128157T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4698T>A	ENSP00000415650.3:p.Ala1566=
ENST00000457135.2:c.907T>A
ENST00000334344.11:c.4698T>A MANE Select	ENSP00000335044.6:p.Ala1566=
ENST00000422737.6:c.4619T>A
ENST00000334344.10:c.4698T>A	ENSP00000335044.6:p.Ala1566=
ENST00000422737.5:c.4251T>A	ENSP00000415650.1:p.Ala1417=
ENST00000444670.5:c.3528T>A	ENSP00000397307.1:p.Ala1176=
ENST00000457135.1:c.522T>A	ENSP00000388357.1:p.Ala174=
ENST00000479608.5:n.3989T>A
NM_152641.2:c.4698T>A	NP_689854.2:p.Ala1566=
XM_006719272.2:c.4698T>A	XP_006719335.1:p.Ala1566=
XM_011538025.1:c.3066T>A	XP_011536327.1:p.Ala1022=
XR_944505.1:n.4846T>A
NM_001347839.1:c.4698T>A	NP_001334768.1:p.Ala1566=
NM_152641.3:c.4698T>A	NP_689854.2:p.Ala1566=
XM_006719272.4:c.4698T>A	XP_006719335.1:p.Ala1566=
XR_944505.3:n.4829T>A
NM_152641.4:c.4698T>A MANE Select	NP_689854.2:p.Ala1566=
NM_001347839.2:c.4698T>A	NP_001334768.1:p.Ala1566=