Canonical Allele Identifier: CA2634409724

Gene: WWOX

Linked Data

• gnomAD v4: 16-78099510-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099510T>G , CM000678.2:g.78099510T>G	GRCh38
NC_000016.9:g.78133407T>G , CM000678.1:g.78133407T>G	GRCh37
NC_000016.8:g.76690908T>G	NCBI36
NG_011698.1:g.4857T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-269T>G	ENSP00000485925.2:n.-269T>G
ENST00000682609.1:n.59T>G
ENST00000683286.1:n.59T>G
ENST00000683929.1:c.-269T>G	ENSP00000507689.1:n.-269T>G
ENST00000684070.1:n.61T>G
ENST00000684381.1:n.59T>G
ENST00000684452.1:n.59T>G
ENST00000684632.1:n.111T>G
ENST00000566780.5:c.-269T>G	ENSP00000457230.1:n.-269T>G
ENST00000627394.2:c.-269T>G	ENSP00000485925.1:n.-269T>G
NM_001291997.1:c.-543T>G	NP_001278926.1:n.-543T>G
NM_016373.3:c.-269T>G	NP_057457.1:n.-269T>G
NM_130791.3:c.-269T>G	NP_570607.1:n.-269T>G
NR_120435.1:n.98T>G
NR_120436.1:n.98T>G