Canonical Allele Identifier: CA724256922

Gene: WWOX

Linked Data

• dbSNP Id: rs1285550897
• gnomAD v3: 16-78099563-T-C
• gnomAD v4: 16-78099563-T-C
• MyVariant Identifiers: chr16:g.78133460T>C (hg19) ; chr16:g.78099563T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099563T>C , CM000678.2:g.78099563T>C	GRCh38
NC_000016.9:g.78133460T>C , CM000678.1:g.78133460T>C	GRCh37
NC_000016.8:g.76690961T>C	NCBI36
NG_011698.1:g.4910T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-216T>C	ENSP00000485925.2:n.-216T>C
ENST00000682609.1:n.112T>C
ENST00000683286.1:n.112T>C
ENST00000683929.1:c.-216T>C	ENSP00000507689.1:n.-216T>C
ENST00000684070.1:n.114T>C
ENST00000684381.1:n.112T>C
ENST00000684452.1:n.112T>C
ENST00000684632.1:n.164T>C
ENST00000566780.5:c.-216T>C	ENSP00000457230.1:n.-216T>C
ENST00000627394.2:c.-216T>C	ENSP00000485925.1:n.-216T>C
NM_001291997.1:c.-490T>C	NP_001278926.1:n.-490T>C
NM_016373.3:c.-216T>C	NP_057457.1:n.-216T>C
NM_130791.3:c.-216T>C	NP_570607.1:n.-216T>C
NR_120435.1:n.151T>C
NR_120436.1:n.151T>C