Canonical Allele Identifier: CA284501417
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs1036774335
gnomAD v2: 16-78133308-G-C
gnomAD v3: 16-78099411-G-C
gnomAD v4: 16-78099411-G-C
MyVariant Identifiers: chr16:g.78133308G>C (hg19) chr16:g.78099411G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099411G>C , CM000678.2:g.78099411G>C GRCh38
NC_000016.9:g.78133308G>C , CM000678.1:g.78133308G>C GRCh37
NC_000016.8:g.76690809G>C NCBI36
NG_011698.1:g.4758G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-368G>C ENSP00000485925.2:n.-368G>C
ENST00000683929.1:c.-368G>C ENSP00000507689.1:n.-368G>C
ENST00000684632.1:n.12G>C
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