Canonical Allele Identifier: CA2634409654
Gene: WWOX HGNC NCBI

Linked Data

gnomAD v4: 16-78099449-T-C
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Genomic Alleles

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

Transcript Alleles

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