Canonical Allele Identifier: CA8183504

Gene: WWOX

Linked Data

• ClinVar Variation Id: 967434
• ClinVar RCV Id: RCV001242345 ; RCV003156326
• dbSNP Id: rs756228469
• ExAC: 16:78466411 G / A
• gnomAD v2: 16-78466411-G-A
• gnomAD v3: 16-78432514-G-A
• gnomAD v4: 16-78432514-G-A
• MyVariant Identifiers: chr16:g.78466411G>A (hg19) ; chr16:g.78432514G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432514G>A , CM000678.2:g.78432514G>A	GRCh38
NC_000016.9:g.78466411G>A , CM000678.1:g.78466411G>A	GRCh37
NC_000016.8:g.77023912G>A	NCBI36
NG_011698.1:g.337861G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.818G>A	ENSP00000485925.2:p.Gly273Glu
ENST00000683929.1:c.818G>A	ENSP00000507689.1:p.Gly273Glu
ENST00000684632.1:n.1197G>A
ENST00000566780.6:c.818G>A MANE Select	ENSP00000457230.1:p.Gly273Glu
ENST00000402655.6:c.409+317360G>A	ENSP00000384238.2:n.409+317360G>A
ENST00000406884.6:c.516+268225G>A	ENSP00000384495.2:n.516+268225G>A
ENST00000408984.7:c.818G>A	ENSP00000386161.3:p.Gly273Glu
ENST00000539474.6:c.409+317360G>A	ENSP00000445210.2:n.409+317360G>A
ENST00000562639.5:n.506G>A
ENST00000566780.5:c.818G>A	ENSP00000457230.1:p.Gly273Glu
ENST00000569332.5:c.*615G>A	ENSP00000454788.1:n.*615G>A
ENST00000620008.1:c.212G>A	ENSP00000482648.1:p.Gly71Glu
NM_001291997.1:c.479G>A	NP_001278926.1:p.Gly160Glu
NM_016373.3:c.818G>A	NP_057457.1:p.Gly273Glu
XM_006721195.2:c.818G>A	XP_006721258.1:p.Gly273Glu
XM_011523100.1:c.818G>A	XP_011521402.1:p.Gly273Glu
XM_011523101.1:c.818G>A	XP_011521403.1:p.Gly273Glu
XM_011523102.1:c.818G>A	XP_011521404.1:p.Gly273Glu
XM_011523103.1:c.818G>A	XP_011521405.1:p.Gly273Glu
XM_011523104.1:c.818G>A	XP_011521406.1:p.Gly273Glu
XR_933765.1:n.3419-1701C>T
XM_011523101.3:c.818G>A	XP_011521403.1:p.Gly273Glu
XM_011523103.3:c.818G>A	XP_011521405.1:p.Gly273Glu
XM_011523104.3:c.818G>A	XP_011521406.1:p.Gly273Glu
NM_016373.4:c.818G>A MANE Select	NP_057457.1:p.Gly273Glu
NM_001291997.2:c.479G>A	NP_001278926.1:p.Gly160Glu