Canonical Allele Identifier: CA6526670
Gene: ARID2 HGNC NCBI

Linked Data

dbSNP Id: rs762564588

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852616C>T , CM000674.2:g.45852616C>T GRCh38
NC_000012.11:g.46246399C>T , CM000674.1:g.46246399C>T GRCh37
NC_000012.10:g.44532666C>T NCBI36
NG_052800.1:g.127952C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4493C>T ENSP00000415650.3:p.Ala1498Val
ENST00000457135.2:c.702C>T
ENST00000334344.11:c.4493C>T MANE Select ENSP00000335044.6:p.Ala1498Val
ENST00000422737.6:c.4414C>T
ENST00000334344.10:c.4493C>T ENSP00000335044.6:p.Ala1498Val
ENST00000422737.5:c.4046C>T ENSP00000415650.1:p.Ala1349Val
ENST00000444670.5:c.3323C>T ENSP00000397307.1:p.Ala1108Val
ENST00000457135.1:c.317C>T ENSP00000388357.1:p.Ala106Val
ENST00000479608.5:n.3784C>T
NM_152641.2:c.4493C>T NP_689854.2:p.Ala1498Val
XM_006719272.2:c.4493C>T XP_006719335.1:p.Ala1498Val
XM_011538025.1:c.2861C>T XP_011536327.1:p.Ala954Val
XR_944505.1:n.4641C>T
NM_001347839.1:c.4493C>T NP_001334768.1:p.Ala1498Val
NM_152641.3:c.4493C>T NP_689854.2:p.Ala1498Val
XM_006719272.4:c.4493C>T XP_006719335.1:p.Ala1498Val
XR_944505.3:n.4624C>T
NM_152641.4:c.4493C>T MANE Select NP_689854.2:p.Ala1498Val
NM_001347839.2:c.4493C>T NP_001334768.1:p.Ala1498Val