Canonical Allele Identifier: CA384452312

Gene: ARID2

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45904933G>C , CM000674.2:g.45904933G>C	GRCh38
NC_000012.11:g.46298716G>C , CM000674.1:g.46298716G>C	GRCh37
NC_000012.10:g.44584983G>C	NCBI36
NG_052800.1:g.180269G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457135.2:c.1630-1G>C
ENST00000334344.11:c.5364-1G>C MANE Select	ENSP00000335044.6:n.5364-1G>C
ENST00000334344.10:c.5364-1G>C	ENSP00000335044.6:n.5364-1G>C
ENST00000444670.5:c.4194-1G>C	ENSP00000397307.1:n.4194-1G>C
ENST00000457135.1:c.*39-1G>C	ENSP00000388357.1:n.*39-1G>C
ENST00000479608.5:n.4655-1G>C
NM_152641.2:c.5364-1G>C	NP_689854.2:n.5364-1G>C
XM_006719272.2:c.*39-1G>C	XP_006719335.1:n.*39-1G>C
XM_011538025.1:c.3732-1G>C	XP_011536327.1:n.3732-1G>C
XR_944505.1:n.5570-1G>C
NM_152641.3:c.5364-1G>C	NP_689854.2:n.5364-1G>C
XM_006719272.4:c.*39-1G>C	XP_006719335.1:n.*39-1G>C
XR_944505.3:n.5553-1G>C
NM_152641.4:c.5364-1G>C MANE Select	NP_689854.2:n.5364-1G>C