Canonical Allele Identifier: CA384492220

Gene: ARID2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4669C>G	ENSP00000415650.3:p.Pro1557Ala
ENST00000457135.2:c.878C>G
ENST00000334344.11:c.4669C>G MANE Select	ENSP00000335044.6:p.Pro1557Ala
ENST00000422737.6:c.4590C>G
ENST00000334344.10:c.4669C>G	ENSP00000335044.6:p.Pro1557Ala
ENST00000422737.5:c.4222C>G	ENSP00000415650.1:p.Pro1408Ala
ENST00000444670.5:c.3499C>G	ENSP00000397307.1:p.Pro1167Ala
ENST00000457135.1:c.493C>G	ENSP00000388357.1:p.Pro165Ala
ENST00000479608.5:n.3960C>G
NM_152641.2:c.4669C>G	NP_689854.2:p.Pro1557Ala
XM_006719272.2:c.4669C>G	XP_006719335.1:p.Pro1557Ala
XM_011538025.1:c.3037C>G	XP_011536327.1:p.Pro1013Ala
XR_944505.1:n.4817C>G
NM_001347839.1:c.4669C>G	NP_001334768.1:p.Pro1557Ala
NM_152641.3:c.4669C>G	NP_689854.2:p.Pro1557Ala
XM_006719272.4:c.4669C>G	XP_006719335.1:p.Pro1557Ala
XR_944505.3:n.4800C>G
NM_152641.4:c.4669C>G MANE Select	NP_689854.2:p.Pro1557Ala
NM_001347839.2:c.4669C>G	NP_001334768.1:p.Pro1557Ala