Canonical Allele Identifier: CA2634409715

Gene: WWOX

Linked Data

• gnomAD v4: 16-78099501-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099501T>A , CM000678.2:g.78099501T>A	GRCh38
NC_000016.9:g.78133398T>A , CM000678.1:g.78133398T>A	GRCh37
NC_000016.8:g.76690899T>A	NCBI36
NG_011698.1:g.4848T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-278T>A	ENSP00000485925.2:n.-278T>A
ENST00000682609.1:n.50T>A
ENST00000683286.1:n.50T>A
ENST00000683929.1:c.-278T>A	ENSP00000507689.1:n.-278T>A
ENST00000684070.1:n.52T>A
ENST00000684381.1:n.50T>A
ENST00000684452.1:n.50T>A
ENST00000684632.1:n.102T>A
ENST00000566780.5:c.-278T>A	ENSP00000457230.1:n.-278T>A
ENST00000627394.2:c.-278T>A	ENSP00000485925.1:n.-278T>A
NM_001291997.1:c.-552T>A	NP_001278926.1:n.-552T>A
NM_016373.3:c.-278T>A	NP_057457.1:n.-278T>A
NM_130791.3:c.-278T>A	NP_570607.1:n.-278T>A
NR_120435.1:n.89T>A
NR_120436.1:n.89T>A