Canonical Allele Identifier: CA656671663
Gene: WWOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099437A>T , CM000678.2:g.78099437A>T GRCh38
NC_000016.9:g.78133334A>T , CM000678.1:g.78133334A>T GRCh37
NC_000016.8:g.76690835A>T NCBI36
NG_011698.1:g.4784A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-342A>T ENSP00000485925.2:n.-342A>T
ENST00000683929.1:c.-342A>T ENSP00000507689.1:n.-342A>T
ENST00000684632.1:n.38A>T
ENST00000566780.5:c.-342A>T ENSP00000457230.1:n.-342A>T
ENST00000627394.2:c.-342A>T ENSP00000485925.1:n.-342A>T
NM_001291997.1:c.-616A>T NP_001278926.1:n.-616A>T
NM_016373.3:c.-342A>T NP_057457.1:n.-342A>T
NM_130791.3:c.-342A>T NP_570607.1:n.-342A>T
NR_120435.1:n.25A>T
NR_120436.1:n.25A>T