Canonical Allele Identifier: CA384492123

Gene: ARID2

Linked Data

• dbSNP Id: rs2138181100
• MyVariant Identifiers: chr12:g.46246533G>C (hg19) ; chr12:g.45852750G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852750G>C , CM000674.2:g.45852750G>C	GRCh38
NC_000012.11:g.46246533G>C , CM000674.1:g.46246533G>C	GRCh37
NC_000012.10:g.44532800G>C	NCBI36
NG_052800.1:g.128086G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4627G>C	ENSP00000415650.3:p.Asp1543His
ENST00000457135.2:c.836G>C
ENST00000334344.11:c.4627G>C MANE Select	ENSP00000335044.6:p.Asp1543His
ENST00000422737.6:c.4548G>C
ENST00000334344.10:c.4627G>C	ENSP00000335044.6:p.Asp1543His
ENST00000422737.5:c.4180G>C	ENSP00000415650.1:p.Asp1394His
ENST00000444670.5:c.3457G>C	ENSP00000397307.1:p.Asp1153His
ENST00000457135.1:c.451G>C	ENSP00000388357.1:p.Asp151His
ENST00000479608.5:n.3918G>C
NM_152641.2:c.4627G>C	NP_689854.2:p.Asp1543His
XM_006719272.2:c.4627G>C	XP_006719335.1:p.Asp1543His
XM_011538025.1:c.2995G>C	XP_011536327.1:p.Asp999His
XR_944505.1:n.4775G>C
NM_001347839.1:c.4627G>C	NP_001334768.1:p.Asp1543His
NM_152641.3:c.4627G>C	NP_689854.2:p.Asp1543His
XM_006719272.4:c.4627G>C	XP_006719335.1:p.Asp1543His
XR_944505.3:n.4758G>C
NM_152641.4:c.4627G>C MANE Select	NP_689854.2:p.Asp1543His
NM_001347839.2:c.4627G>C	NP_001334768.1:p.Asp1543His