Canonical Allele Identifier: CA384492222

Gene: ARID2

Linked Data

• dbSNP Id: rs2138181472
• MyVariant Identifiers: chr12:g.46246575C>T (hg19) ; chr12:g.45852792C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852792C>T , CM000674.2:g.45852792C>T	GRCh38
NC_000012.11:g.46246575C>T , CM000674.1:g.46246575C>T	GRCh37
NC_000012.10:g.44532842C>T	NCBI36
NG_052800.1:g.128128C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4669C>T	ENSP00000415650.3:p.Pro1557Ser
ENST00000457135.2:c.878C>T
ENST00000334344.11:c.4669C>T MANE Select	ENSP00000335044.6:p.Pro1557Ser
ENST00000422737.6:c.4590C>T
ENST00000334344.10:c.4669C>T	ENSP00000335044.6:p.Pro1557Ser
ENST00000422737.5:c.4222C>T	ENSP00000415650.1:p.Pro1408Ser
ENST00000444670.5:c.3499C>T	ENSP00000397307.1:p.Pro1167Ser
ENST00000457135.1:c.493C>T	ENSP00000388357.1:p.Pro165Ser
ENST00000479608.5:n.3960C>T
NM_152641.2:c.4669C>T	NP_689854.2:p.Pro1557Ser
XM_006719272.2:c.4669C>T	XP_006719335.1:p.Pro1557Ser
XM_011538025.1:c.3037C>T	XP_011536327.1:p.Pro1013Ser
XR_944505.1:n.4817C>T
NM_001347839.1:c.4669C>T	NP_001334768.1:p.Pro1557Ser
NM_152641.3:c.4669C>T	NP_689854.2:p.Pro1557Ser
XM_006719272.4:c.4669C>T	XP_006719335.1:p.Pro1557Ser
XR_944505.3:n.4800C>T
NM_152641.4:c.4669C>T MANE Select	NP_689854.2:p.Pro1557Ser
NM_001347839.2:c.4669C>T	NP_001334768.1:p.Pro1557Ser