Canonical Allele Identifier: CA384492171

Gene: ARID2

Linked Data

• dbSNP Id: rs1024679911
• MyVariant Identifiers: chr12:g.46246554A>T (hg19) ; chr12:g.45852771A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852771A>T , CM000674.2:g.45852771A>T	GRCh38
NC_000012.11:g.46246554A>T , CM000674.1:g.46246554A>T	GRCh37
NC_000012.10:g.44532821A>T	NCBI36
NG_052800.1:g.128107A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4648A>T	ENSP00000415650.3:p.Ser1550Cys
ENST00000457135.2:c.857A>T
ENST00000334344.11:c.4648A>T MANE Select	ENSP00000335044.6:p.Ser1550Cys
ENST00000422737.6:c.4569A>T
ENST00000334344.10:c.4648A>T	ENSP00000335044.6:p.Ser1550Cys
ENST00000422737.5:c.4201A>T	ENSP00000415650.1:p.Ser1401Cys
ENST00000444670.5:c.3478A>T	ENSP00000397307.1:p.Ser1160Cys
ENST00000457135.1:c.472A>T	ENSP00000388357.1:p.Ser158Cys
ENST00000479608.5:n.3939A>T
NM_152641.2:c.4648A>T	NP_689854.2:p.Ser1550Cys
XM_006719272.2:c.4648A>T	XP_006719335.1:p.Ser1550Cys
XM_011538025.1:c.3016A>T	XP_011536327.1:p.Ser1006Cys
XR_944505.1:n.4796A>T
NM_001347839.1:c.4648A>T	NP_001334768.1:p.Ser1550Cys
NM_152641.3:c.4648A>T	NP_689854.2:p.Ser1550Cys
XM_006719272.4:c.4648A>T	XP_006719335.1:p.Ser1550Cys
XR_944505.3:n.4779A>T
NM_152641.4:c.4648A>T MANE Select	NP_689854.2:p.Ser1550Cys
NM_001347839.2:c.4648A>T	NP_001334768.1:p.Ser1550Cys