Canonical Allele Identifier: CA284501399
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs565260365
gnomAD v3: 16-78099401-G-A
gnomAD v4: 16-78099401-G-A
MyVariant Identifiers: chr16:g.78133298G>A (hg19) chr16:g.78099401G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099401G>A , CM000678.2:g.78099401G>A GRCh38
NC_000016.9:g.78133298G>A , CM000678.1:g.78133298G>A GRCh37
NC_000016.8:g.76690799G>A NCBI36
NG_011698.1:g.4748G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-378G>A ENSP00000485925.2:n.-378G>A
ENST00000683929.1:c.-378G>A ENSP00000507689.1:n.-378G>A
ENST00000684632.1:n.2G>A
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