Canonical Allele Identifier: CA2634409613
Gene: WWOX HGNC NCBI

Linked Data

gnomAD v4: 16-78099412-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099412A>C , CM000678.2:g.78099412A>C GRCh38
NC_000016.9:g.78133309A>C , CM000678.1:g.78133309A>C GRCh37
NC_000016.8:g.76690810A>C NCBI36
NG_011698.1:g.4759A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-367A>C ENSP00000485925.2:n.-367A>C
ENST00000683929.1:c.-367A>C ENSP00000507689.1:n.-367A>C
ENST00000684632.1:n.13A>C
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