Canonical Allele Identifier: CA2234888420
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099414T= , CM000678.2:g.78099414T= GRCh38
NC_000016.9:g.78133311T= , CM000678.1:g.78133311T= GRCh37
NC_000016.8:g.76690812T= NCBI36
NG_011698.1:g.4761T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-365T= ENSP00000485925.2:n.-365T=
ENST00000683929.1:c.-365T= ENSP00000507689.1:n.-365T=
ENST00000684632.1:n.15T=
ENST00000566780.5:c.-365T= ENSP00000457230.1:n.-365T=
NM_001291997.1:c.-639T= NP_001278926.1:n.-639T=
NM_016373.3:c.-365T= NP_057457.1:n.-365T=
NM_130791.3:c.-365T= NP_570607.1:n.-365T=
NR_120435.1:n.2T=
NR_120436.1:n.2T=