Canonical Allele Identifier: CA8182971
Gene: WWOX HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 260735
dbSNP Id: rs11545028

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099774C>T , CM000678.2:g.78099774C>T GRCh38
NC_000016.9:g.78133671C>T , CM000678.1:g.78133671C>T GRCh37
NC_000016.8:g.76691172C>T NCBI36
NG_011698.1:g.5121C>T

Transcript Alleles

HGVS Amino-acid change
NM_001291997.1:c.-279C>T VV NP_001278926.1:p.=
NM_016373.3:c.-5C>T VV NP_057457.1:p.=
NM_130791.3:c.-5C>T VV NP_570607.1:p.=
NR_120435.1:n.362C>T
NR_120436.1:n.362C>T
XM_006721195.2:c.-5C>T XP_006721258.1:p.=
XM_011523100.1:c.-5C>T XP_011521402.1:p.=
XM_011523101.1:c.-5C>T XP_011521403.1:p.=
XM_011523102.1:c.-5C>T XP_011521404.1:p.=
XM_011523103.1:c.-5C>T XP_011521405.1:p.=
XM_011523104.1:c.-5C>T XP_011521406.1:p.=
XM_011523105.1:c.-5C>T XP_011521407.1:p.=
XM_011523101.3:c.-5C>T
XM_011523103.3:c.-5C>T
XM_011523104.3:c.-5C>T
XM_011523105.3:c.-5C>T
XM_017023278.2:c.-5C>T XP_016878767.1:p.=
ENST00000355860.7:c.-5C>T ENSP00000348119.3:p.=
ENST00000402655.6:c.-5C>T ENSP00000384238.2:p.=
ENST00000406884.6:c.-5C>T ENSP00000384495.2:p.=
ENST00000408984.7:c.-5C>T ENSP00000386161.3:p.=
ENST00000539474.6:c.-5C>T ENSP00000445210.2:p.=
ENST00000561846.5:n.40C>T
ENST00000562214.5:n.119C>T
ENST00000565562.5:n.41C>T
ENST00000566662.5:c.-5C>T ENSP00000454331.1:p.=
ENST00000566780.5:c.-5C>T ENSP00000457230.1:p.=
ENST00000569332.5:c.-5C>T ENSP00000454788.1:p.=
ENST00000569818.1:c.-5C>T ENSP00000454485.1:p.=
ENST00000627394.2:c.-5C>T ENSP00000485925.1:p.=