Canonical Allele Identifier: CA724256962

Gene: WWOX

Linked Data

• dbSNP Id: rs1489552725
• gnomAD v4: 16-78099631-C-G
• MyVariant Identifiers: chr16:g.78133528C>G (hg19) ; chr16:g.78099631C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099631C>G , CM000678.2:g.78099631C>G	GRCh38
NC_000016.9:g.78133528C>G , CM000678.1:g.78133528C>G	GRCh37
NC_000016.8:g.76691029C>G	NCBI36
NG_011698.1:g.4978C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-148C>G	ENSP00000485925.2:n.-148C>G
ENST00000682609.1:n.180C>G
ENST00000683286.1:n.180C>G
ENST00000683929.1:c.-148C>G	ENSP00000507689.1:n.-148C>G
ENST00000684070.1:n.182C>G
ENST00000684381.1:n.180C>G
ENST00000684452.1:n.180C>G
ENST00000684632.1:n.232C>G
ENST00000566780.5:c.-148C>G	ENSP00000457230.1:n.-148C>G
ENST00000569332.5:c.-148C>G	ENSP00000454788.1:n.-148C>G
ENST00000627394.2:c.-148C>G	ENSP00000485925.1:n.-148C>G
NM_001291997.1:c.-422C>G	NP_001278926.1:n.-422C>G
NM_016373.3:c.-148C>G	NP_057457.1:n.-148C>G
NM_130791.3:c.-148C>G	NP_570607.1:n.-148C>G
NR_120435.1:n.219C>G
NR_120436.1:n.219C>G