Canonical Allele Identifier: CA284501506

Gene: WWOX

Linked Data

• dbSNP Id: rs117763255
• gnomAD v2: 16-78133350-G-A
• gnomAD v3: 16-78099453-G-A
• gnomAD v4: 16-78099453-G-A
• MyVariant Identifiers: chr16:g.78133350G>A (hg19) ; chr16:g.78099453G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099453G>A , CM000678.2:g.78099453G>A	GRCh38
NC_000016.9:g.78133350G>A , CM000678.1:g.78133350G>A	GRCh37
NC_000016.8:g.76690851G>A	NCBI36
NG_011698.1:g.4800G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-326G>A	ENSP00000485925.2:n.-326G>A
ENST00000682609.1:n.2G>A
ENST00000683286.1:n.2G>A
ENST00000683929.1:c.-326G>A	ENSP00000507689.1:n.-326G>A
ENST00000684070.1:n.4G>A
ENST00000684381.1:n.2G>A
ENST00000684452.1:n.2G>A
ENST00000684632.1:n.54G>A
ENST00000566780.5:c.-326G>A	ENSP00000457230.1:n.-326G>A
ENST00000627394.2:c.-326G>A	ENSP00000485925.1:n.-326G>A
NM_001291997.1:c.-600G>A	NP_001278926.1:n.-600G>A
NM_016373.3:c.-326G>A	NP_057457.1:n.-326G>A
NM_130791.3:c.-326G>A	NP_570607.1:n.-326G>A
NR_120435.1:n.41G>A
NR_120436.1:n.41G>A