Canonical Allele Identifier: CA384491742

Gene: ARID2

Linked Data

• dbSNP Id: rs749439841
• MyVariant Identifiers: chr12:g.46246354T>G (hg19) ; chr12:g.45852571T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852571T>G , CM000674.2:g.45852571T>G	GRCh38
NC_000012.11:g.46246354T>G , CM000674.1:g.46246354T>G	GRCh37
NC_000012.10:g.44532621T>G	NCBI36
NG_052800.1:g.127907T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000422737.7:c.4448T>G	ENSP00000415650.3:p.Ile1483Ser
ENST00000457135.2:c.657T>G
ENST00000334344.11:c.4448T>G MANE Select	ENSP00000335044.6:p.Ile1483Ser
ENST00000422737.6:c.4369T>G
ENST00000334344.10:c.4448T>G	ENSP00000335044.6:p.Ile1483Ser
ENST00000422737.5:c.4001T>G	ENSP00000415650.1:p.Ile1334Ser
ENST00000444670.5:c.3278T>G	ENSP00000397307.1:p.Ile1093Ser
ENST00000457135.1:c.272T>G	ENSP00000388357.1:p.Ile91Ser
ENST00000479608.5:n.3739T>G
NM_152641.2:c.4448T>G	NP_689854.2:p.Ile1483Ser
XM_006719272.2:c.4448T>G	XP_006719335.1:p.Ile1483Ser
XM_011538025.1:c.2816T>G	XP_011536327.1:p.Ile939Ser
XR_944505.1:n.4596T>G
NM_001347839.1:c.4448T>G	NP_001334768.1:p.Ile1483Ser
NM_152641.3:c.4448T>G	NP_689854.2:p.Ile1483Ser
XM_006719272.4:c.4448T>G	XP_006719335.1:p.Ile1483Ser
XR_944505.3:n.4579T>G
NM_152641.4:c.4448T>G MANE Select	NP_689854.2:p.Ile1483Ser
NM_001347839.2:c.4448T>G	NP_001334768.1:p.Ile1483Ser