Canonical Allele Identifier: CA2732872926
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs2151650882
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099400A>G , CM000678.2:g.78099400A>G GRCh38
NC_000016.9:g.78133297A>G , CM000678.1:g.78133297A>G GRCh37
NC_000016.8:g.76690798A>G NCBI36
NG_011698.1:g.4747A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-379A>G ENSP00000485925.2:n.-379A>G
ENST00000683929.1:c.-379A>G ENSP00000507689.1:n.-379A>G
ENST00000684632.1:n.1A>G
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