Canonical Allele Identifier: CA2234888592
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs2031596387

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099521C>T , CM000678.2:g.78099521C>T GRCh38
NC_000016.9:g.78133418C>T , CM000678.1:g.78133418C>T GRCh37
NC_000016.8:g.76690919C>T NCBI36
NG_011698.1:g.4868C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-258C>T ENSP00000485925.2:n.-258C>T
ENST00000682609.1:n.70C>T
ENST00000683286.1:n.70C>T
ENST00000683929.1:c.-258C>T ENSP00000507689.1:n.-258C>T
ENST00000684070.1:n.72C>T
ENST00000684381.1:n.70C>T
ENST00000684452.1:n.70C>T
ENST00000684632.1:n.122C>T
ENST00000566780.5:c.-258C>T ENSP00000457230.1:n.-258C>T
ENST00000627394.2:c.-258C>T ENSP00000485925.1:n.-258C>T
NM_001291997.1:c.-532C>T NP_001278926.1:n.-532C>T
NM_016373.3:c.-258C>T NP_057457.1:n.-258C>T
NM_130791.3:c.-258C>T NP_570607.1:n.-258C>T
NR_120435.1:n.109C>T
NR_120436.1:n.109C>T