Canonical Allele Identifier: CA384453127

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45836896C>T , CM000674.2:g.45836896C>T	GRCh38
NC_000012.11:g.46230679C>T , CM000674.1:g.46230679C>T	GRCh37
NC_000012.10:g.44516946C>T	NCBI36
NG_052800.1:g.112232C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.928C>T	ENSP00000415650.3:p.Arg310Cys
ENST00000334344.11:c.928C>T MANE Select	ENSP00000335044.6:p.Arg310Cys
ENST00000422737.6:c.849C>T
ENST00000334344.10:c.928C>T	ENSP00000335044.6:p.Arg310Cys
ENST00000422737.5:c.481C>T	ENSP00000415650.1:p.Arg161Cys
ENST00000479608.5:n.136C>T
NM_152641.2:c.928C>T	NP_689854.2:p.Arg310Cys
XM_006719272.2:c.928C>T	XP_006719335.1:p.Arg310Cys
XR_944505.1:n.1076C>T
XR_944892.1:n.289+2956G>A
XR_944893.1:n.290-2011G>A
NM_001347839.1:c.928C>T	NP_001334768.1:p.Arg310Cys
NM_152641.3:c.928C>T	NP_689854.2:p.Arg310Cys
XM_006719272.4:c.928C>T	XP_006719335.1:p.Arg310Cys
XR_001749098.1:n.476+2956G>A
XR_944505.3:n.1059C>T
XR_944892.2:n.289+2956G>A
NM_152641.4:c.928C>T MANE Select	NP_689854.2:p.Arg310Cys
NM_001347839.2:c.928C>T	NP_001334768.1:p.Arg310Cys