Canonical Allele Identifier: CA8183558

Gene: WWOX

Linked Data

• dbSNP Id: rs765339835
• ExAC: 16:78466522 G / A
• gnomAD v2: 16-78466522-G-A
• gnomAD v3: 16-78432625-G-A
• gnomAD v4: 16-78432625-G-A
• COSMIC: COSM2692629 ; COSM2692630
• MyVariant Identifiers: chr16:g.78466522G>A (hg19) ; chr16:g.78432625G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432625G>A , CM000678.2:g.78432625G>A	GRCh38
NC_000016.9:g.78466522G>A , CM000678.1:g.78466522G>A	GRCh37
NC_000016.8:g.77024023G>A	NCBI36
NG_011698.1:g.337972G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.929G>A	ENSP00000485925.2:p.Arg310His
ENST00000683929.1:c.929G>A	ENSP00000507689.1:p.Arg310His
ENST00000684632.1:n.1308G>A
ENST00000566780.6:c.929G>A MANE Select	ENSP00000457230.1:p.Arg310His
ENST00000402655.6:c.409+317471G>A	ENSP00000384238.2:n.409+317471G>A
ENST00000406884.6:c.516+268336G>A	ENSP00000384495.2:n.516+268336G>A
ENST00000408984.7:c.929G>A	ENSP00000386161.3:p.Arg310His
ENST00000539474.6:c.409+317471G>A	ENSP00000445210.2:n.409+317471G>A
ENST00000566780.5:c.929G>A	ENSP00000457230.1:p.Arg310His
ENST00000569332.5:c.*726G>A	ENSP00000454788.1:n.*726G>A
ENST00000620008.1:c.323G>A	ENSP00000482648.1:p.Arg108His
NM_001291997.1:c.590G>A	NP_001278926.1:p.Arg197His
NM_016373.3:c.929G>A	NP_057457.1:p.Arg310His
XM_006721195.2:c.929G>A	XP_006721258.1:p.Arg310His
XM_011523100.1:c.929G>A	XP_011521402.1:p.Arg310His
XM_011523101.1:c.929G>A	XP_011521403.1:p.Arg310His
XM_011523102.1:c.929G>A	XP_011521404.1:p.Arg310His
XM_011523103.1:c.929G>A	XP_011521405.1:p.Arg310His
XM_011523104.1:c.929G>A	XP_011521406.1:p.Arg310His
XR_933765.1:n.3418+1695C>T
XM_011523101.3:c.929G>A	XP_011521403.1:p.Arg310His
XM_011523103.3:c.929G>A	XP_011521405.1:p.Arg310His
XM_011523104.3:c.929G>A	XP_011521406.1:p.Arg310His
NM_016373.4:c.929G>A MANE Select	NP_057457.1:p.Arg310His
NM_001291997.2:c.590G>A	NP_001278926.1:p.Arg197His