Canonical Allele Identifier: CA479694147

Gene: ARID2

Linked Data

• MyVariant Identifiers: chr12:g.46246547T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852764T>C , CM000674.2:g.45852764T>C	GRCh38
NC_000012.11:g.46246547T>C , CM000674.1:g.46246547T>C	GRCh37
NC_000012.10:g.44532814T>C	NCBI36
NG_052800.1:g.128100T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4641T>C	ENSP00000415650.3:p.Ala1547=
ENST00000457135.2:c.850T>C
ENST00000334344.11:c.4641T>C MANE Select	ENSP00000335044.6:p.Ala1547=
ENST00000422737.6:c.4562T>C
ENST00000334344.10:c.4641T>C	ENSP00000335044.6:p.Ala1547=
ENST00000422737.5:c.4194T>C	ENSP00000415650.1:p.Ala1398=
ENST00000444670.5:c.3471T>C	ENSP00000397307.1:p.Ala1157=
ENST00000457135.1:c.465T>C	ENSP00000388357.1:p.Ala155=
ENST00000479608.5:n.3932T>C
NM_152641.2:c.4641T>C	NP_689854.2:p.Ala1547=
XM_006719272.2:c.4641T>C	XP_006719335.1:p.Ala1547=
XM_011538025.1:c.3009T>C	XP_011536327.1:p.Ala1003=
XR_944505.1:n.4789T>C
NM_001347839.1:c.4641T>C	NP_001334768.1:p.Ala1547=
NM_152641.3:c.4641T>C	NP_689854.2:p.Ala1547=
XM_006719272.4:c.4641T>C	XP_006719335.1:p.Ala1547=
XR_944505.3:n.4772T>C
NM_152641.4:c.4641T>C MANE Select	NP_689854.2:p.Ala1547=
NM_001347839.2:c.4641T>C	NP_001334768.1:p.Ala1547=