Canonical Allele Identifier: CA2634409729

Gene: WWOX

Linked Data

• gnomAD v4: 16-78099517-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099517C>A , CM000678.2:g.78099517C>A	GRCh38
NC_000016.9:g.78133414C>A , CM000678.1:g.78133414C>A	GRCh37
NC_000016.8:g.76690915C>A	NCBI36
NG_011698.1:g.4864C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-262C>A	ENSP00000485925.2:n.-262C>A
ENST00000682609.1:n.66C>A
ENST00000683286.1:n.66C>A
ENST00000683929.1:c.-262C>A	ENSP00000507689.1:n.-262C>A
ENST00000684070.1:n.68C>A
ENST00000684381.1:n.66C>A
ENST00000684452.1:n.66C>A
ENST00000684632.1:n.118C>A
ENST00000566780.5:c.-262C>A	ENSP00000457230.1:n.-262C>A
ENST00000627394.2:c.-262C>A	ENSP00000485925.1:n.-262C>A
NM_001291997.1:c.-536C>A	NP_001278926.1:n.-536C>A
NM_016373.3:c.-262C>A	NP_057457.1:n.-262C>A
NM_130791.3:c.-262C>A	NP_570607.1:n.-262C>A
NR_120435.1:n.105C>A
NR_120436.1:n.105C>A