Canonical Allele Identifier: CA2234888417
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099413G= , CM000678.2:g.78099413G= GRCh38
NC_000016.9:g.78133310G= , CM000678.1:g.78133310G= GRCh37
NC_000016.8:g.76690811G= NCBI36
NG_011698.1:g.4760G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-366G= ENSP00000485925.2:n.-366G=
ENST00000683929.1:c.-366G= ENSP00000507689.1:n.-366G=
ENST00000684632.1:n.14G=
ENST00000566780.5:c.-366G= ENSP00000457230.1:n.-366G=
NM_001291997.1:c.-640G= NP_001278926.1:n.-640G=
NM_016373.3:c.-366G= NP_057457.1:n.-366G=
NM_130791.3:c.-366G= NP_570607.1:n.-366G=
NR_120435.1:n.1G=
NR_120436.1:n.1G=