Canonical Allele Identifier: CA2234888465
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs2031588102
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099449T>G , CM000678.2:g.78099449T>G GRCh38
NC_000016.9:g.78133346T>G , CM000678.1:g.78133346T>G GRCh37
NC_000016.8:g.76690847T>G NCBI36
NG_011698.1:g.4796T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-330T>G ENSP00000485925.2:n.-330T>G
ENST00000683929.1:c.-330T>G ENSP00000507689.1:n.-330T>G
ENST00000684632.1:n.50T>G
ENST00000566780.5:c.-330T>G ENSP00000457230.1:n.-330T>G
ENST00000627394.2:c.-330T>G ENSP00000485925.1:n.-330T>G
NM_001291997.1:c.-604T>G NP_001278926.1:n.-604T>G
NM_016373.3:c.-330T>G NP_057457.1:n.-330T>G
NM_130791.3:c.-330T>G NP_570607.1:n.-330T>G
NR_120435.1:n.37T>G
NR_120436.1:n.37T>G
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