Canonical Allele Identifier: CA979326675
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs986544645
gnomAD v3: 16-78099408-G-C
gnomAD v4: 16-78099408-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099408G>C , CM000678.2:g.78099408G>C GRCh38
NC_000016.9:g.78133305G>C , CM000678.1:g.78133305G>C GRCh37
NC_000016.8:g.76690806G>C NCBI36
NG_011698.1:g.4755G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-371G>C ENSP00000485925.2:n.-371G>C
ENST00000683929.1:c.-371G>C ENSP00000507689.1:n.-371G>C
ENST00000684632.1:n.9G>C
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