Canonical Allele Identifier: CA2234888595
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099522C= , CM000678.2:g.78099522C= GRCh38
NC_000016.9:g.78133419C= , CM000678.1:g.78133419C= GRCh37
NC_000016.8:g.76690920C= NCBI36
NG_011698.1:g.4869C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-257C= ENSP00000485925.2:n.-257C=
ENST00000682609.1:n.71C=
ENST00000683286.1:n.71C=
ENST00000683929.1:c.-257C= ENSP00000507689.1:n.-257C=
ENST00000684070.1:n.73C=
ENST00000684381.1:n.71C=
ENST00000684452.1:n.71C=
ENST00000684632.1:n.123C=
ENST00000566780.5:c.-257C= ENSP00000457230.1:n.-257C=
ENST00000627394.2:c.-257C= ENSP00000485925.1:n.-257C=
NM_001291997.1:c.-531C= NP_001278926.1:n.-531C=
NM_016373.3:c.-257C= NP_057457.1:n.-257C=
NM_130791.3:c.-257C= NP_570607.1:n.-257C=
NR_120435.1:n.110C=
NR_120436.1:n.110C=