Canonical Allele Identifier: CA10588626
Gene: WWOX HGNC NCBI

Linked Data

ClinVar Variation Id: 265596
ClinVar RCV Id: RCV000255229
dbSNP Id: rs886039653
MyVariant Identifiers: chr16:g.78198079G>A (hg19) chr16:g.78164182G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78164182G>A , CM000678.2:g.78164182G>A GRCh38
NC_000016.9:g.78198079G>A , CM000678.1:g.78198079G>A GRCh37
NC_000016.8:g.76755580G>A NCBI36
NG_011698.1:g.69529G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000627394.3:c.410-1G>A ENSP00000485925.2:n.410-1G>A
ENST00000683286.1:n.737-1G>A
ENST00000683929.1:c.410-1G>A ENSP00000507689.1:n.410-1G>A
ENST00000684070.1:n.674-1G>A
ENST00000684632.1:n.789-1G>A
ENST00000566780.6:c.410-1G>A MANE Select ENSP00000457230.1:n.410-1G>A
ENST00000355860.7:c.410-1G>A ENSP00000348119.3:n.410-1G>A
ENST00000402655.6:c.409+49028G>A ENSP00000384238.2:n.409+49028G>A
ENST00000406884.6:c.410-1G>A ENSP00000384495.2:n.410-1G>A
ENST00000408984.7:c.410-1G>A ENSP00000386161.3:n.410-1G>A
ENST00000539474.6:c.409+49028G>A ENSP00000445210.2:n.409+49028G>A
ENST00000561846.5:n.454-1G>A
ENST00000562639.5:n.98-1G>A
ENST00000563358.5:n.517-1G>A
ENST00000565791.1:n.18-1G>A
ENST00000566662.5:c.*28-1G>A ENSP00000454331.1:n.*28-1G>A
ENST00000566780.5:c.410-1G>A ENSP00000457230.1:n.410-1G>A
ENST00000569332.5:c.*207-1G>A ENSP00000454788.1:n.*207-1G>A
ENST00000627394.2:c.*207-1G>A ENSP00000485925.1:n.*207-1G>A
NM_001291997.1:c.71-1G>A NP_001278926.1:n.71-1G>A
NM_016373.3:c.410-1G>A NP_057457.1:n.410-1G>A
NM_130791.3:c.410-1G>A NP_570607.1:n.410-1G>A
NR_120436.1:n.890-1G>A
XM_006721195.2:c.410-1G>A XP_006721258.1:n.410-1G>A
XM_011523100.1:c.410-1G>A XP_011521402.1:n.410-1G>A
XM_011523101.1:c.410-1G>A XP_011521403.1:n.410-1G>A
XM_011523102.1:c.410-1G>A XP_011521404.1:n.410-1G>A
XM_011523103.1:c.410-1G>A XP_011521405.1:n.410-1G>A
XM_011523104.1:c.410-1G>A XP_011521406.1:n.410-1G>A
XM_011523105.1:c.410-1G>A XP_011521407.1:n.410-1G>A
XM_011523101.3:c.410-1G>A XP_011521403.1:n.410-1G>A
XM_011523103.3:c.410-1G>A XP_011521405.1:n.410-1G>A
XM_011523104.3:c.410-1G>A XP_011521406.1:n.410-1G>A
XM_011523105.3:c.410-1G>A XP_011521407.1:n.410-1G>A
XM_017023278.2:c.410-1G>A XP_016878767.1:n.410-1G>A
NM_016373.4:c.410-1G>A MANE Select NP_057457.1:n.410-1G>A
NM_001291997.2:c.71-1G>A NP_001278926.1:n.71-1G>A
NM_130791.4:c.410-1G>A NP_570607.1:n.410-1G>A
NR_120436.2:n.649-1G>A
NM_130791.5:c.410-1G>A NP_570607.1:n.410-1G>A
NR_120436.3:n.649-1G>A
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