Canonical Allele Identifier: CA979326745

Gene: WWOX

Linked Data

• dbSNP Id: rs2031595608
• gnomAD v3: 16-78099513-C-T
• gnomAD v4: 16-78099513-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099513C>T , CM000678.2:g.78099513C>T	GRCh38
NC_000016.9:g.78133410C>T , CM000678.1:g.78133410C>T	GRCh37
NC_000016.8:g.76690911C>T	NCBI36
NG_011698.1:g.4860C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-266C>T	ENSP00000485925.2:n.-266C>T
ENST00000682609.1:n.62C>T
ENST00000683286.1:n.62C>T
ENST00000683929.1:c.-266C>T	ENSP00000507689.1:n.-266C>T
ENST00000684070.1:n.64C>T
ENST00000684381.1:n.62C>T
ENST00000684452.1:n.62C>T
ENST00000684632.1:n.114C>T
ENST00000566780.5:c.-266C>T	ENSP00000457230.1:n.-266C>T
ENST00000627394.2:c.-266C>T	ENSP00000485925.1:n.-266C>T
NM_001291997.1:c.-540C>T	NP_001278926.1:n.-540C>T
NM_016373.3:c.-266C>T	NP_057457.1:n.-266C>T
NM_130791.3:c.-266C>T	NP_570607.1:n.-266C>T
NR_120435.1:n.101C>T
NR_120436.1:n.101C>T