Canonical Allele Identifier: CA384491692

Gene: ARID2

Linked Data

• MyVariant Identifiers: chr12:g.46246347C>A (hg19) ; chr12:g.45852564C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852564C>A , CM000674.2:g.45852564C>A	GRCh38
NC_000012.11:g.46246347C>A , CM000674.1:g.46246347C>A	GRCh37
NC_000012.10:g.44532614C>A	NCBI36
NG_052800.1:g.127900C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4441C>A	ENSP00000415650.3:p.His1481Asn
ENST00000457135.2:c.650C>A
ENST00000334344.11:c.4441C>A MANE Select	ENSP00000335044.6:p.His1481Asn
ENST00000422737.6:c.4362C>A
ENST00000334344.10:c.4441C>A	ENSP00000335044.6:p.His1481Asn
ENST00000422737.5:c.3994C>A	ENSP00000415650.1:p.His1332Asn
ENST00000444670.5:c.3271C>A	ENSP00000397307.1:p.His1091Asn
ENST00000457135.1:c.265C>A	ENSP00000388357.1:p.His89Asn
ENST00000479608.5:n.3732C>A
NM_152641.2:c.4441C>A	NP_689854.2:p.His1481Asn
XM_006719272.2:c.4441C>A	XP_006719335.1:p.His1481Asn
XM_011538025.1:c.2809C>A	XP_011536327.1:p.His937Asn
XR_944505.1:n.4589C>A
NM_001347839.1:c.4441C>A	NP_001334768.1:p.His1481Asn
NM_152641.3:c.4441C>A	NP_689854.2:p.His1481Asn
XM_006719272.4:c.4441C>A	XP_006719335.1:p.His1481Asn
XR_944505.3:n.4572C>A
NM_152641.4:c.4441C>A MANE Select	NP_689854.2:p.His1481Asn
NM_001347839.2:c.4441C>A	NP_001334768.1:p.His1481Asn