Canonical Allele Identifier: CA2634409685
Gene: WWOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099467A>G , CM000678.2:g.78099467A>G GRCh38
NC_000016.9:g.78133364A>G , CM000678.1:g.78133364A>G GRCh37
NC_000016.8:g.76690865A>G NCBI36
NG_011698.1:g.4814A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-312A>G ENSP00000485925.2:n.-312A>G
ENST00000682609.1:n.16A>G
ENST00000683286.1:n.16A>G
ENST00000683929.1:c.-312A>G ENSP00000507689.1:n.-312A>G
ENST00000684070.1:n.18A>G
ENST00000684381.1:n.16A>G
ENST00000684452.1:n.16A>G
ENST00000684632.1:n.68A>G
ENST00000566780.5:c.-312A>G ENSP00000457230.1:n.-312A>G
ENST00000627394.2:c.-312A>G ENSP00000485925.1:n.-312A>G
NM_001291997.1:c.-586A>G NP_001278926.1:n.-586A>G
NM_016373.3:c.-312A>G NP_057457.1:n.-312A>G
NM_130791.3:c.-312A>G NP_570607.1:n.-312A>G
NR_120435.1:n.55A>G
NR_120436.1:n.55A>G