Canonical Allele Identifier: CA2634409651
Gene: WWOX HGNC NCBI

Linked Data

gnomAD v4: 16-78099446-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099446C>A , CM000678.2:g.78099446C>A GRCh38
NC_000016.9:g.78133343C>A , CM000678.1:g.78133343C>A GRCh37
NC_000016.8:g.76690844C>A NCBI36
NG_011698.1:g.4793C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-333C>A ENSP00000485925.2:n.-333C>A
ENST00000683929.1:c.-333C>A ENSP00000507689.1:n.-333C>A
ENST00000684632.1:n.47C>A
ENST00000566780.5:c.-333C>A ENSP00000457230.1:n.-333C>A
ENST00000627394.2:c.-333C>A ENSP00000485925.1:n.-333C>A
NM_001291997.1:c.-607C>A NP_001278926.1:n.-607C>A
NM_016373.3:c.-333C>A NP_057457.1:n.-333C>A
NM_130791.3:c.-333C>A NP_570607.1:n.-333C>A
NR_120435.1:n.34C>A
NR_120436.1:n.34C>A
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