Canonical Allele Identifier: CA2033475785
Gene: ARID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45852819G= , CM000674.2:g.45852819G= GRCh38
NC_000012.11:g.46246602G= , CM000674.1:g.46246602G= GRCh37
NC_000012.10:g.44532869G= NCBI36
NG_052800.1:g.128155G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000422737.7:c.4696G= ENSP00000415650.3:p.Ala1566=
ENST00000457135.2:c.905G=
ENST00000334344.11:c.4696G= MANE Select ENSP00000335044.6:p.Ala1566=
ENST00000422737.6:c.4617G=
ENST00000334344.10:c.4696G= ENSP00000335044.6:p.Ala1566=
ENST00000422737.5:c.4249G= ENSP00000415650.1:p.Ala1417=
ENST00000444670.5:c.3526G= ENSP00000397307.1:p.Ala1176=
ENST00000457135.1:c.520G= ENSP00000388357.1:p.Ala174=
ENST00000479608.5:n.3987G=
NM_152641.2:c.4696G= NP_689854.2:p.Ala1566=
XM_006719272.2:c.4696G= XP_006719335.1:p.Ala1566=
XM_011538025.1:c.3064G= XP_011536327.1:p.Ala1022=
XR_944505.1:n.4844G=
NM_001347839.1:c.4696G= NP_001334768.1:p.Ala1566=
NM_152641.3:c.4696G= NP_689854.2:p.Ala1566=
XM_006719272.4:c.4696G= XP_006719335.1:p.Ala1566=
XR_944505.3:n.4827G=
NM_152641.4:c.4696G= MANE Select NP_689854.2:p.Ala1566=
NM_001347839.2:c.4696G= NP_001334768.1:p.Ala1566=