Canonical Allele Identifier: CA2634409784
Gene: WWOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099571C>A , CM000678.2:g.78099571C>A GRCh38
NC_000016.9:g.78133468C>A , CM000678.1:g.78133468C>A GRCh37
NC_000016.8:g.76690969C>A NCBI36
NG_011698.1:g.4918C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-208C>A ENSP00000485925.2:n.-208C>A
ENST00000682609.1:n.120C>A
ENST00000683286.1:n.120C>A
ENST00000683929.1:c.-208C>A ENSP00000507689.1:n.-208C>A
ENST00000684070.1:n.122C>A
ENST00000684381.1:n.120C>A
ENST00000684452.1:n.120C>A
ENST00000684632.1:n.172C>A
ENST00000566780.5:c.-208C>A ENSP00000457230.1:n.-208C>A
ENST00000627394.2:c.-208C>A ENSP00000485925.1:n.-208C>A
NM_001291997.1:c.-482C>A NP_001278926.1:n.-482C>A
NM_016373.3:c.-208C>A NP_057457.1:n.-208C>A
NM_130791.3:c.-208C>A NP_570607.1:n.-208C>A
NR_120435.1:n.159C>A
NR_120436.1:n.159C>A