Canonical Allele Identifier: CA724256766
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs1193462128
gnomAD v3: 16-78099402-C-T
gnomAD v4: 16-78099402-C-T
MyVariant Identifiers: chr16:g.78133299C>T (hg19) chr16:g.78099402C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099402C>T , CM000678.2:g.78099402C>T GRCh38
NC_000016.9:g.78133299C>T , CM000678.1:g.78133299C>T GRCh37
NC_000016.8:g.76690800C>T NCBI36
NG_011698.1:g.4749C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-377C>T ENSP00000485925.2:n.-377C>T
ENST00000683929.1:c.-377C>T ENSP00000507689.1:n.-377C>T
ENST00000684632.1:n.3C>T
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