Canonical Allele Identifier: CA285033511

Gene: WWOX

Linked Data

• dbSNP Id: rs7190925
• gnomAD v2: 16-78569869-C-G
• gnomAD v3: 16-78535972-C-G
• gnomAD v4: 16-78535972-C-G
• MyVariant Identifiers: chr16:g.78569869C>G (hg19) ; chr16:g.78535972C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78535972C>G , CM000678.2:g.78535972C>G	GRCh38
NC_000016.9:g.78569869C>G , CM000678.1:g.78569869C>G	GRCh37
NC_000016.8:g.77127370C>G	NCBI36
NG_011698.1:g.441319C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.1152+130C>G	ENSP00000485925.2:n.1152+130C>G
ENST00000683929.1:c.1056+103220C>G	ENSP00000507689.1:n.1056+103220C>G
ENST00000684632.1:n.1436-99875C>G
ENST00000566780.6:c.1056+103220C>G MANE Select	ENSP00000457230.1:n.1056+103220C>G
ENST00000402655.6:c.409+420818C>G	ENSP00000384238.2:n.409+420818C>G
ENST00000406884.6:c.516+371683C>G	ENSP00000384495.2:n.516+371683C>G
ENST00000408984.7:c.1056+103220C>G	ENSP00000386161.3:n.1056+103220C>G
ENST00000539474.6:c.410-220968C>G	ENSP00000445210.2:n.410-220968C>G
ENST00000566780.5:c.1056+103220C>G	ENSP00000457230.1:n.1056+103220C>G
ENST00000569332.5:c.*853+103220C>G	ENSP00000454788.1:n.*853+103220C>G
NM_001291997.1:c.717+103220C>G	NP_001278926.1:n.717+103220C>G
NM_016373.3:c.1056+103220C>G	NP_057457.1:n.1056+103220C>G
XM_011523100.1:c.1152+130C>G	XP_011521402.1:n.1152+130C>G
XM_011523101.1:c.1057-38087C>G	XP_011521403.1:n.1057-38087C>G
XM_011523103.1:c.1056+103220C>G	XP_011521405.1:n.1056+103220C>G
XM_011523101.3:c.1057-38087C>G	XP_011521403.1:n.1057-38087C>G
XM_011523103.3:c.1056+103220C>G	XP_011521405.1:n.1056+103220C>G
XM_017023279.1:c.142+130C>G	XP_016878768.1:n.142+130C>G
NM_016373.4:c.1056+103220C>G MANE Select	NP_057457.1:n.1056+103220C>G
NM_001291997.2:c.717+103220C>G	NP_001278926.1:n.717+103220C>G