Canonical Allele Identifier: CA979326687

Gene: WWOX

Linked Data

• dbSNP Id: rs1347152464
• gnomAD v3: 16-78099427-C-G
• gnomAD v4: 16-78099427-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099427C>G , CM000678.2:g.78099427C>G	GRCh38
NC_000016.9:g.78133324C>G , CM000678.1:g.78133324C>G	GRCh37
NC_000016.8:g.76690825C>G	NCBI36
NG_011698.1:g.4774C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-352C>G	ENSP00000485925.2:n.-352C>G
ENST00000683929.1:c.-352C>G	ENSP00000507689.1:n.-352C>G
ENST00000684632.1:n.28C>G
ENST00000566780.5:c.-352C>G	ENSP00000457230.1:n.-352C>G
NM_001291997.1:c.-626C>G	NP_001278926.1:n.-626C>G
NM_016373.3:c.-352C>G	NP_057457.1:n.-352C>G
NM_130791.3:c.-352C>G	NP_570607.1:n.-352C>G
NR_120435.1:n.15C>G
NR_120436.1:n.15C>G