Canonical Allele Identifier: CA396843291

Gene: WWOX

Linked Data

• ClinVar Variation Id: 1524720
• ClinVar RCV Id: RCV002031926
• dbSNP Id: rs2151386107
• gnomAD v4: 16-78432619-A-G
• MyVariant Identifiers: chr16:g.78466516A>G (hg19) ; chr16:g.78432619A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432619A>G , CM000678.2:g.78432619A>G	GRCh38
NC_000016.9:g.78466516A>G , CM000678.1:g.78466516A>G	GRCh37
NC_000016.8:g.77024017A>G	NCBI36
NG_011698.1:g.337966A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.923A>G	ENSP00000485925.2:p.His308Arg
ENST00000683929.1:c.923A>G	ENSP00000507689.1:p.His308Arg
ENST00000684632.1:n.1302A>G
ENST00000566780.6:c.923A>G MANE Select	ENSP00000457230.1:p.His308Arg
ENST00000402655.6:c.409+317465A>G	ENSP00000384238.2:n.409+317465A>G
ENST00000406884.6:c.516+268330A>G	ENSP00000384495.2:n.516+268330A>G
ENST00000408984.7:c.923A>G	ENSP00000386161.3:p.His308Arg
ENST00000539474.6:c.409+317465A>G	ENSP00000445210.2:n.409+317465A>G
ENST00000566780.5:c.923A>G	ENSP00000457230.1:p.His308Arg
ENST00000569332.5:c.*720A>G	ENSP00000454788.1:n.*720A>G
ENST00000620008.1:c.317A>G	ENSP00000482648.1:p.His106Arg
NM_001291997.1:c.584A>G	NP_001278926.1:p.His195Arg
NM_016373.3:c.923A>G	NP_057457.1:p.His308Arg
XM_006721195.2:c.923A>G	XP_006721258.1:p.His308Arg
XM_011523100.1:c.923A>G	XP_011521402.1:p.His308Arg
XM_011523101.1:c.923A>G	XP_011521403.1:p.His308Arg
XM_011523102.1:c.923A>G	XP_011521404.1:p.His308Arg
XM_011523103.1:c.923A>G	XP_011521405.1:p.His308Arg
XM_011523104.1:c.923A>G	XP_011521406.1:p.His308Arg
XR_933765.1:n.3418+1701T>C
XM_011523101.3:c.923A>G	XP_011521403.1:p.His308Arg
XM_011523103.3:c.923A>G	XP_011521405.1:p.His308Arg
XM_011523104.3:c.923A>G	XP_011521406.1:p.His308Arg
NM_016373.4:c.923A>G MANE Select	NP_057457.1:p.His308Arg
NM_001291997.2:c.584A>G	NP_001278926.1:p.His195Arg