Canonical Allele Identifier: CA479693768

Gene: ARID2

Linked Data

• dbSNP Id: rs2138179169
• MyVariant Identifiers: chr12:g.46246271T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852488T>C , CM000674.2:g.45852488T>C	GRCh38
NC_000012.11:g.46246271T>C , CM000674.1:g.46246271T>C	GRCh37
NC_000012.10:g.44532538T>C	NCBI36
NG_052800.1:g.127824T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4365T>C	ENSP00000415650.3:p.Ser1455=
ENST00000457135.2:c.574T>C
ENST00000334344.11:c.4365T>C MANE Select	ENSP00000335044.6:p.Ser1455=
ENST00000422737.6:c.4286T>C
ENST00000334344.10:c.4365T>C	ENSP00000335044.6:p.Ser1455=
ENST00000422737.5:c.3918T>C	ENSP00000415650.1:p.Ser1306=
ENST00000444670.5:c.3195T>C	ENSP00000397307.1:p.Ser1065=
ENST00000457135.1:c.189T>C	ENSP00000388357.1:p.Ser63=
ENST00000479608.5:n.3656T>C
NM_152641.2:c.4365T>C	NP_689854.2:p.Ser1455=
XM_006719272.2:c.4365T>C	XP_006719335.1:p.Ser1455=
XM_011538025.1:c.2733T>C	XP_011536327.1:p.Ser911=
XR_944505.1:n.4513T>C
NM_001347839.1:c.4365T>C	NP_001334768.1:p.Ser1455=
NM_152641.3:c.4365T>C	NP_689854.2:p.Ser1455=
XM_006719272.4:c.4365T>C	XP_006719335.1:p.Ser1455=
XR_944505.3:n.4496T>C
NM_152641.4:c.4365T>C MANE Select	NP_689854.2:p.Ser1455=
NM_001347839.2:c.4365T>C	NP_001334768.1:p.Ser1455=