Canonical Allele Identifier: CA979326673
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs2031582825

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099404del , CM000678.2:g.78099404del GRCh38
NC_000016.9:g.78133301del , CM000678.1:g.78133301del GRCh37
NC_000016.8:g.76690802del NCBI36
NG_011698.1:g.4751del

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-375del ENSP00000485925.2:n.-375del
ENST00000683929.1:c.-375del ENSP00000507689.1:n.-375del
ENST00000684632.1:n.5del