Canonical Allele Identifier: CA2234888456
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs2031587424

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099441C>T , CM000678.2:g.78099441C>T GRCh38
NC_000016.9:g.78133338C>T , CM000678.1:g.78133338C>T GRCh37
NC_000016.8:g.76690839C>T NCBI36
NG_011698.1:g.4788C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-338C>T ENSP00000485925.2:n.-338C>T
ENST00000683929.1:c.-338C>T ENSP00000507689.1:n.-338C>T
ENST00000684632.1:n.42C>T
ENST00000566780.5:c.-338C>T ENSP00000457230.1:n.-338C>T
ENST00000627394.2:c.-338C>T ENSP00000485925.1:n.-338C>T
NM_001291997.1:c.-612C>T NP_001278926.1:n.-612C>T
NM_016373.3:c.-338C>T NP_057457.1:n.-338C>T
NM_130791.3:c.-338C>T NP_570607.1:n.-338C>T
NR_120435.1:n.29C>T
NR_120436.1:n.29C>T