Canonical Allele Identifier: CA2569619281
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099460G>T , CM000678.2:g.78099460G>T GRCh38
NC_000016.9:g.78133357G>T , CM000678.1:g.78133357G>T GRCh37
NC_000016.8:g.76690858G>T NCBI36
NG_011698.1:g.4807G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-319G>T ENSP00000485925.2:n.-319G>T
ENST00000682609.1:n.9G>T
ENST00000683286.1:n.9G>T
ENST00000683929.1:c.-319G>T ENSP00000507689.1:n.-319G>T
ENST00000684070.1:n.11G>T
ENST00000684381.1:n.9G>T
ENST00000684452.1:n.9G>T
ENST00000684632.1:n.61G>T
ENST00000566780.5:c.-319G>T ENSP00000457230.1:n.-319G>T
ENST00000627394.2:c.-319G>T ENSP00000485925.1:n.-319G>T
NM_001291997.1:c.-593G>T NP_001278926.1:n.-593G>T
NM_016373.3:c.-319G>T NP_057457.1:n.-319G>T
NM_130791.3:c.-319G>T NP_570607.1:n.-319G>T
NR_120435.1:n.48G>T
NR_120436.1:n.48G>T