Canonical Allele Identifier: CA6526697

Gene: ARID2

Linked Data

• dbSNP Id: rs752665033
• ExAC: 12:46246543 A / C
• gnomAD v2: 12-46246543-A-C
• gnomAD v4: 12-45852760-A-C
• MyVariant Identifiers: chr12:g.46246543A>C (hg19) ; chr12:g.45852760A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852760A>C , CM000674.2:g.45852760A>C	GRCh38
NC_000012.11:g.46246543A>C , CM000674.1:g.46246543A>C	GRCh37
NC_000012.10:g.44532810A>C	NCBI36
NG_052800.1:g.128096A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4637A>C	ENSP00000415650.3:p.Asn1546Thr
ENST00000457135.2:c.846A>C
ENST00000334344.11:c.4637A>C MANE Select	ENSP00000335044.6:p.Asn1546Thr
ENST00000422737.6:c.4558A>C
ENST00000334344.10:c.4637A>C	ENSP00000335044.6:p.Asn1546Thr
ENST00000422737.5:c.4190A>C	ENSP00000415650.1:p.Asn1397Thr
ENST00000444670.5:c.3467A>C	ENSP00000397307.1:p.Asn1156Thr
ENST00000457135.1:c.461A>C	ENSP00000388357.1:p.Asn154Thr
ENST00000479608.5:n.3928A>C
NM_152641.2:c.4637A>C	NP_689854.2:p.Asn1546Thr
XM_006719272.2:c.4637A>C	XP_006719335.1:p.Asn1546Thr
XM_011538025.1:c.3005A>C	XP_011536327.1:p.Asn1002Thr
XR_944505.1:n.4785A>C
NM_001347839.1:c.4637A>C	NP_001334768.1:p.Asn1546Thr
NM_152641.3:c.4637A>C	NP_689854.2:p.Asn1546Thr
XM_006719272.4:c.4637A>C	XP_006719335.1:p.Asn1546Thr
XR_944505.3:n.4768A>C
NM_152641.4:c.4637A>C MANE Select	NP_689854.2:p.Asn1546Thr
NM_001347839.2:c.4637A>C	NP_001334768.1:p.Asn1546Thr