Canonical Allele Identifier: CA384492438

Gene: ARID2

Linked Data

• dbSNP Id: rs1943581696
• MyVariant Identifiers: chr12:g.46246615T>C (hg19) ; chr12:g.45852832T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852832T>C , CM000674.2:g.45852832T>C	GRCh38
NC_000012.11:g.46246615T>C , CM000674.1:g.46246615T>C	GRCh37
NC_000012.10:g.44532882T>C	NCBI36
NG_052800.1:g.128168T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4709T>C	ENSP00000415650.3:p.Ile1570Thr
ENST00000457135.2:c.918T>C
ENST00000334344.11:c.4709T>C MANE Select	ENSP00000335044.6:p.Ile1570Thr
ENST00000422737.6:c.4630T>C
ENST00000334344.10:c.4709T>C	ENSP00000335044.6:p.Ile1570Thr
ENST00000422737.5:c.4262T>C	ENSP00000415650.1:p.Ile1421Thr
ENST00000444670.5:c.3539T>C	ENSP00000397307.1:p.Ile1180Thr
ENST00000457135.1:c.533T>C	ENSP00000388357.1:p.Ile178Thr
ENST00000479608.5:n.4000T>C
NM_152641.2:c.4709T>C	NP_689854.2:p.Ile1570Thr
XM_006719272.2:c.4709T>C	XP_006719335.1:p.Ile1570Thr
XM_011538025.1:c.3077T>C	XP_011536327.1:p.Ile1026Thr
XR_944505.1:n.4857T>C
NM_001347839.1:c.4709T>C	NP_001334768.1:p.Ile1570Thr
NM_152641.3:c.4709T>C	NP_689854.2:p.Ile1570Thr
XM_006719272.4:c.4709T>C	XP_006719335.1:p.Ile1570Thr
XR_944505.3:n.4840T>C
NM_152641.4:c.4709T>C MANE Select	NP_689854.2:p.Ile1570Thr
NM_001347839.2:c.4709T>C	NP_001334768.1:p.Ile1570Thr