Canonical Allele Identifier: CA979326949
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs2031618743

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099748A>G , CM000678.2:g.78099748A>G GRCh38
NC_000016.9:g.78133645A>G , CM000678.1:g.78133645A>G GRCh37
NC_000016.8:g.76691146A>G NCBI36
NG_011698.1:g.5095A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-31A>G ENSP00000485925.2:n.-31A>G
ENST00000682609.1:n.297A>G
ENST00000683286.1:n.297A>G
ENST00000683929.1:c.-31A>G ENSP00000507689.1:n.-31A>G
ENST00000684070.1:n.299A>G
ENST00000684381.1:n.297A>G
ENST00000684452.1:n.297A>G
ENST00000684632.1:n.349A>G
ENST00000566780.6:c.-31A>G MANE Select ENSP00000457230.1:n.-31A>G
ENST00000355860.7:c.-31A>G ENSP00000348119.3:n.-31A>G
ENST00000402655.6:c.-31A>G ENSP00000384238.2:n.-31A>G
ENST00000406884.6:c.-31A>G ENSP00000384495.2:n.-31A>G
ENST00000408984.7:c.-31A>G ENSP00000386161.3:n.-31A>G
ENST00000539474.6:c.-31A>G ENSP00000445210.2:n.-31A>G
ENST00000561846.5:n.14A>G
ENST00000562214.5:n.93A>G
ENST00000565562.5:n.15A>G
ENST00000566662.5:c.-31A>G ENSP00000454331.1:n.-31A>G
ENST00000566780.5:c.-31A>G ENSP00000457230.1:n.-31A>G
ENST00000569332.5:c.-31A>G ENSP00000454788.1:n.-31A>G
ENST00000569818.1:c.-31A>G ENSP00000454485.1:n.-31A>G
ENST00000627394.2:c.-31A>G ENSP00000485925.1:n.-31A>G
NM_001291997.1:c.-305A>G NP_001278926.1:n.-305A>G
NM_016373.3:c.-31A>G NP_057457.1:n.-31A>G
NM_130791.3:c.-31A>G NP_570607.1:n.-31A>G
NR_120435.1:n.336A>G
NR_120436.1:n.336A>G
XM_006721195.2:c.-31A>G XP_006721258.1:n.-31A>G
XM_011523100.1:c.-31A>G XP_011521402.1:n.-31A>G
XM_011523101.1:c.-31A>G XP_011521403.1:n.-31A>G
XM_011523102.1:c.-31A>G XP_011521404.1:n.-31A>G
XM_011523103.1:c.-31A>G XP_011521405.1:n.-31A>G
XM_011523104.1:c.-31A>G XP_011521406.1:n.-31A>G
XM_011523105.1:c.-31A>G XP_011521407.1:n.-31A>G
XM_011523101.3:c.-31A>G XP_011521403.1:n.-31A>G
XM_011523103.3:c.-31A>G XP_011521405.1:n.-31A>G
XM_011523104.3:c.-31A>G XP_011521406.1:n.-31A>G
XM_011523105.3:c.-31A>G XP_011521407.1:n.-31A>G
XM_017023278.2:c.-31A>G XP_016878767.1:n.-31A>G
NM_016373.4:c.-31A>G MANE Select NP_057457.1:n.-31A>G
NM_001291997.2:c.-305A>G NP_001278926.1:n.-305A>G
NM_130791.4:c.-31A>G NP_570607.1:n.-31A>G
NR_120435.2:n.95A>G
NR_120436.2:n.95A>G
NM_130791.5:c.-31A>G NP_570607.1:n.-31A>G
NR_120436.3:n.95A>G