Canonical Allele Identifier: CA8182973

Gene: WWOX

Linked Data

• ClinVar Variation Id: 1898392
• ClinVar RCV Id: RCV002570027
• dbSNP Id: rs758588684
• ExAC: 16:78133677 T / C
• gnomAD v2: 16-78133677-T-C
• gnomAD v3: 16-78099780-T-C
• gnomAD v4: 16-78099780-T-C
• MyVariant Identifiers: chr16:g.78133677T>C (hg19) ; chr16:g.78099780T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099780T>C , CM000678.2:g.78099780T>C	GRCh38
NC_000016.9:g.78133677T>C , CM000678.1:g.78133677T>C	GRCh37
NC_000016.8:g.76691178T>C	NCBI36
NG_011698.1:g.5127T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.2T>C	ENSP00000485925.2:p.Met1Thr
ENST00000682609.1:n.329T>C
ENST00000683286.1:n.329T>C
ENST00000683929.1:c.2T>C	ENSP00000507689.1:p.Met1Thr
ENST00000684070.1:n.331T>C
ENST00000684381.1:n.329T>C
ENST00000684452.1:n.329T>C
ENST00000684632.1:n.381T>C
ENST00000566780.6:c.2T>C MANE Select	ENSP00000457230.1:p.Met1Thr
ENST00000355860.7:c.2T>C	ENSP00000348119.3:p.Met1Thr
ENST00000402655.6:c.2T>C	ENSP00000384238.2:p.Met1Thr
ENST00000406884.6:c.2T>C	ENSP00000384495.2:p.Met1Thr
ENST00000408984.7:c.2T>C	ENSP00000386161.3:p.Met1Thr
ENST00000539474.6:c.2T>C	ENSP00000445210.2:p.Met1Thr
ENST00000561846.5:n.46T>C
ENST00000562214.5:n.125T>C
ENST00000565562.5:n.47T>C
ENST00000566662.5:c.2T>C	ENSP00000454331.1:p.Met1Thr
ENST00000566780.5:c.2T>C	ENSP00000457230.1:p.Met1Thr
ENST00000569332.5:c.2T>C	ENSP00000454788.1:p.Met1Thr
ENST00000569818.1:c.2T>C	ENSP00000454485.1:p.Met1Thr
ENST00000627394.2:c.2T>C	ENSP00000485925.1:p.Met1Thr
NM_001291997.1:c.-273T>C	NP_001278926.1:n.-273T>C
NM_016373.3:c.2T>C	NP_057457.1:p.Met1Thr
NM_130791.3:c.2T>C	NP_570607.1:p.Met1Thr
NR_120435.1:n.368T>C
NR_120436.1:n.368T>C
XM_006721195.2:c.2T>C	XP_006721258.1:p.Met1Thr
XM_011523100.1:c.2T>C	XP_011521402.1:p.Met1Thr
XM_011523101.1:c.2T>C	XP_011521403.1:p.Met1Thr
XM_011523102.1:c.2T>C	XP_011521404.1:p.Met1Thr
XM_011523103.1:c.2T>C	XP_011521405.1:p.Met1Thr
XM_011523104.1:c.2T>C	XP_011521406.1:p.Met1Thr
XM_011523105.1:c.2T>C	XP_011521407.1:p.Met1Thr
XM_011523101.3:c.2T>C	XP_011521403.1:p.Met1Thr
XM_011523103.3:c.2T>C	XP_011521405.1:p.Met1Thr
XM_011523104.3:c.2T>C	XP_011521406.1:p.Met1Thr
XM_011523105.3:c.2T>C	XP_011521407.1:p.Met1Thr
XM_017023278.2:c.2T>C	XP_016878767.1:p.Met1Thr
NM_016373.4:c.2T>C MANE Select	NP_057457.1:p.Met1Thr
NM_001291997.2:c.-273T>C	NP_001278926.1:n.-273T>C
NM_130791.4:c.2T>C	NP_570607.1:p.Met1Thr
NR_120435.2:n.127T>C
NR_120436.2:n.127T>C
NM_130791.5:c.2T>C	NP_570607.1:p.Met1Thr
NR_120436.3:n.127T>C