Canonical Allele Identifier: CA2234888660
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs2031598782

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099555C>T , CM000678.2:g.78099555C>T GRCh38
NC_000016.9:g.78133452C>T , CM000678.1:g.78133452C>T GRCh37
NC_000016.8:g.76690953C>T NCBI36
NG_011698.1:g.4902C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-224C>T ENSP00000485925.2:n.-224C>T
ENST00000682609.1:n.104C>T
ENST00000683286.1:n.104C>T
ENST00000683929.1:c.-224C>T ENSP00000507689.1:n.-224C>T
ENST00000684070.1:n.106C>T
ENST00000684381.1:n.104C>T
ENST00000684452.1:n.104C>T
ENST00000684632.1:n.156C>T
ENST00000566780.5:c.-224C>T ENSP00000457230.1:n.-224C>T
ENST00000627394.2:c.-224C>T ENSP00000485925.1:n.-224C>T
NM_001291997.1:c.-498C>T NP_001278926.1:n.-498C>T
NM_016373.3:c.-224C>T NP_057457.1:n.-224C>T
NM_130791.3:c.-224C>T NP_570607.1:n.-224C>T
NR_120435.1:n.143C>T
NR_120436.1:n.143C>T