Canonical Allele Identifier: CA2234888428
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs1597188693
gnomAD v4: 16-78099418-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099418G>C , CM000678.2:g.78099418G>C GRCh38
NC_000016.9:g.78133315G>C , CM000678.1:g.78133315G>C GRCh37
NC_000016.8:g.76690816G>C NCBI36
NG_011698.1:g.4765G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-361G>C ENSP00000485925.2:n.-361G>C
ENST00000683929.1:c.-361G>C ENSP00000507689.1:n.-361G>C
ENST00000684632.1:n.19G>C
ENST00000566780.5:c.-361G>C ENSP00000457230.1:n.-361G>C
NM_001291997.1:c.-635G>C NP_001278926.1:n.-635G>C
NM_016373.3:c.-361G>C NP_057457.1:n.-361G>C
NM_130791.3:c.-361G>C NP_570607.1:n.-361G>C
NR_120435.1:n.6G>C
NR_120436.1:n.6G>C
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