Canonical Allele Identifier: CA2234888424
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099417T= , CM000678.2:g.78099417T= GRCh38
NC_000016.9:g.78133314T= , CM000678.1:g.78133314T= GRCh37
NC_000016.8:g.76690815T= NCBI36
NG_011698.1:g.4764T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-362T= ENSP00000485925.2:n.-362T=
ENST00000683929.1:c.-362T= ENSP00000507689.1:n.-362T=
ENST00000684632.1:n.18T=
ENST00000566780.5:c.-362T= ENSP00000457230.1:n.-362T=
NM_001291997.1:c.-636T= NP_001278926.1:n.-636T=
NM_016373.3:c.-362T= NP_057457.1:n.-362T=
NM_130791.3:c.-362T= NP_570607.1:n.-362T=
NR_120435.1:n.5T=
NR_120436.1:n.5T=