Canonical Allele Identifier: CA2234888440
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099430G= , CM000678.2:g.78099430G= GRCh38
NC_000016.9:g.78133327G= , CM000678.1:g.78133327G= GRCh37
NC_000016.8:g.76690828G= NCBI36
NG_011698.1:g.4777G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-349G= ENSP00000485925.2:n.-349G=
ENST00000683929.1:c.-349G= ENSP00000507689.1:n.-349G=
ENST00000684632.1:n.31G=
ENST00000566780.5:c.-349G= ENSP00000457230.1:n.-349G=
ENST00000627394.2:c.-349G= ENSP00000485925.1:n.-349G=
NM_001291997.1:c.-623G= NP_001278926.1:n.-623G=
NM_016373.3:c.-349G= NP_057457.1:n.-349G=
NM_130791.3:c.-349G= NP_570607.1:n.-349G=
NR_120435.1:n.18G=
NR_120436.1:n.18G=