Canonical Allele Identifier: CA285033544
Gene: WWOX HGNC NCBI

Linked Data

dbSNP Id: rs17706989
gnomAD v2: 16-78569957-C-G
gnomAD v3: 16-78536060-C-G
gnomAD v4: 16-78536060-C-G
MyVariant Identifiers: chr16:g.78569957C>G (hg19) chr16:g.78536060C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78536060C>G , CM000678.2:g.78536060C>G GRCh38
NC_000016.9:g.78569957C>G , CM000678.1:g.78569957C>G GRCh37
NC_000016.8:g.77127458C>G NCBI36
NG_011698.1:g.441407C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000627394.3:c.1152+218C>G ENSP00000485925.2:n.1152+218C>G
ENST00000683929.1:c.1056+103308C>G ENSP00000507689.1:n.1056+103308C>G
ENST00000684632.1:n.1436-99787C>G
ENST00000566780.6:c.1056+103308C>G MANE Select ENSP00000457230.1:n.1056+103308C>G
ENST00000402655.6:c.409+420906C>G ENSP00000384238.2:n.409+420906C>G
ENST00000406884.6:c.516+371771C>G ENSP00000384495.2:n.516+371771C>G
ENST00000408984.7:c.1056+103308C>G ENSP00000386161.3:n.1056+103308C>G
ENST00000539474.6:c.410-220880C>G ENSP00000445210.2:n.410-220880C>G
ENST00000566780.5:c.1056+103308C>G ENSP00000457230.1:n.1056+103308C>G
ENST00000569332.5:c.*853+103308C>G ENSP00000454788.1:n.*853+103308C>G
NM_001291997.1:c.717+103308C>G NP_001278926.1:n.717+103308C>G
NM_016373.3:c.1056+103308C>G NP_057457.1:n.1056+103308C>G
XM_011523100.1:c.1152+218C>G XP_011521402.1:n.1152+218C>G
XM_011523101.1:c.1057-37999C>G XP_011521403.1:n.1057-37999C>G
XM_011523103.1:c.1056+103308C>G XP_011521405.1:n.1056+103308C>G
XM_011523101.3:c.1057-37999C>G XP_011521403.1:n.1057-37999C>G
XM_011523103.3:c.1056+103308C>G XP_011521405.1:n.1056+103308C>G
XM_017023279.1:c.142+218C>G XP_016878768.1:n.142+218C>G
NM_016373.4:c.1056+103308C>G MANE Select NP_057457.1:n.1056+103308C>G
NM_001291997.2:c.717+103308C>G NP_001278926.1:n.717+103308C>G
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