Canonical Allele Identifier: CA384492087

Gene: ARID2

Linked Data

• MyVariant Identifiers: chr12:g.46246516G>T (hg19) ; chr12:g.45852733G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852733G>T , CM000674.2:g.45852733G>T	GRCh38
NC_000012.11:g.46246516G>T , CM000674.1:g.46246516G>T	GRCh37
NC_000012.10:g.44532783G>T	NCBI36
NG_052800.1:g.128069G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4610G>T	ENSP00000415650.3:p.Arg1537Ile
ENST00000457135.2:c.819G>T
ENST00000334344.11:c.4610G>T MANE Select	ENSP00000335044.6:p.Arg1537Ile
ENST00000422737.6:c.4531G>T
ENST00000334344.10:c.4610G>T	ENSP00000335044.6:p.Arg1537Ile
ENST00000422737.5:c.4163G>T	ENSP00000415650.1:p.Arg1388Ile
ENST00000444670.5:c.3440G>T	ENSP00000397307.1:p.Arg1147Ile
ENST00000457135.1:c.434G>T	ENSP00000388357.1:p.Arg145Ile
ENST00000479608.5:n.3901G>T
NM_152641.2:c.4610G>T	NP_689854.2:p.Arg1537Ile
XM_006719272.2:c.4610G>T	XP_006719335.1:p.Arg1537Ile
XM_011538025.1:c.2978G>T	XP_011536327.1:p.Arg993Ile
XR_944505.1:n.4758G>T
NM_001347839.1:c.4610G>T	NP_001334768.1:p.Arg1537Ile
NM_152641.3:c.4610G>T	NP_689854.2:p.Arg1537Ile
XM_006719272.4:c.4610G>T	XP_006719335.1:p.Arg1537Ile
XR_944505.3:n.4741G>T
NM_152641.4:c.4610G>T MANE Select	NP_689854.2:p.Arg1537Ile
NM_001347839.2:c.4610G>T	NP_001334768.1:p.Arg1537Ile