Canonical Allele Identifier: CA396843294

Gene: WWOX

Linked Data

• ClinVar Variation Id: 1394690
• ClinVar RCV Id: RCV001900967
• dbSNP Id: rs774296956
• MyVariant Identifiers: chr16:g.78466517C>G (hg19) ; chr16:g.78432620C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78432620C>G , CM000678.2:g.78432620C>G	GRCh38
NC_000016.9:g.78466517C>G , CM000678.1:g.78466517C>G	GRCh37
NC_000016.8:g.77024018C>G	NCBI36
NG_011698.1:g.337967C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000627394.3:c.924C>G	ENSP00000485925.2:p.His308Gln
ENST00000683929.1:c.924C>G	ENSP00000507689.1:p.His308Gln
ENST00000684632.1:n.1303C>G
ENST00000566780.6:c.924C>G MANE Select	ENSP00000457230.1:p.His308Gln
ENST00000402655.6:c.409+317466C>G	ENSP00000384238.2:n.409+317466C>G
ENST00000406884.6:c.516+268331C>G	ENSP00000384495.2:n.516+268331C>G
ENST00000408984.7:c.924C>G	ENSP00000386161.3:p.His308Gln
ENST00000539474.6:c.409+317466C>G	ENSP00000445210.2:n.409+317466C>G
ENST00000566780.5:c.924C>G	ENSP00000457230.1:p.His308Gln
ENST00000569332.5:c.*721C>G	ENSP00000454788.1:n.*721C>G
ENST00000620008.1:c.318C>G	ENSP00000482648.1:p.His106Gln
NM_001291997.1:c.585C>G	NP_001278926.1:p.His195Gln
NM_016373.3:c.924C>G	NP_057457.1:p.His308Gln
XM_006721195.2:c.924C>G	XP_006721258.1:p.His308Gln
XM_011523100.1:c.924C>G	XP_011521402.1:p.His308Gln
XM_011523101.1:c.924C>G	XP_011521403.1:p.His308Gln
XM_011523102.1:c.924C>G	XP_011521404.1:p.His308Gln
XM_011523103.1:c.924C>G	XP_011521405.1:p.His308Gln
XM_011523104.1:c.924C>G	XP_011521406.1:p.His308Gln
XR_933765.1:n.3418+1700G>C
XM_011523101.3:c.924C>G	XP_011521403.1:p.His308Gln
XM_011523103.3:c.924C>G	XP_011521405.1:p.His308Gln
XM_011523104.3:c.924C>G	XP_011521406.1:p.His308Gln
NM_016373.4:c.924C>G MANE Select	NP_057457.1:p.His308Gln
NM_001291997.2:c.585C>G	NP_001278926.1:p.His195Gln