Canonical Allele Identifier: CA2506568387
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099564C>A , CM000678.2:g.78099564C>A GRCh38
NC_000016.9:g.78133461C>A , CM000678.1:g.78133461C>A GRCh37
NC_000016.8:g.76690962C>A NCBI36
NG_011698.1:g.4911C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-215C>A ENSP00000485925.2:n.-215C>A
ENST00000682609.1:n.113C>A
ENST00000683286.1:n.113C>A
ENST00000683929.1:c.-215C>A ENSP00000507689.1:n.-215C>A
ENST00000684070.1:n.115C>A
ENST00000684381.1:n.113C>A
ENST00000684452.1:n.113C>A
ENST00000684632.1:n.165C>A
ENST00000566780.5:c.-215C>A ENSP00000457230.1:n.-215C>A
ENST00000627394.2:c.-215C>A ENSP00000485925.1:n.-215C>A
NM_001291997.1:c.-489C>A NP_001278926.1:n.-489C>A
NM_016373.3:c.-215C>A NP_057457.1:n.-215C>A
NM_130791.3:c.-215C>A NP_570607.1:n.-215C>A
NR_120435.1:n.152C>A
NR_120436.1:n.152C>A