Canonical Allele Identifier: CA2234888581

Gene: WWOX

Linked Data

• dbSNP Id: rs2031595458

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099512G>C , CM000678.2:g.78099512G>C	GRCh38
NC_000016.9:g.78133409G>C , CM000678.1:g.78133409G>C	GRCh37
NC_000016.8:g.76690910G>C	NCBI36
NG_011698.1:g.4859G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-267G>C	ENSP00000485925.2:n.-267G>C
ENST00000682609.1:n.61G>C
ENST00000683286.1:n.61G>C
ENST00000683929.1:c.-267G>C	ENSP00000507689.1:n.-267G>C
ENST00000684070.1:n.63G>C
ENST00000684381.1:n.61G>C
ENST00000684452.1:n.61G>C
ENST00000684632.1:n.113G>C
ENST00000566780.5:c.-267G>C	ENSP00000457230.1:n.-267G>C
ENST00000627394.2:c.-267G>C	ENSP00000485925.1:n.-267G>C
NM_001291997.1:c.-541G>C	NP_001278926.1:n.-541G>C
NM_016373.3:c.-267G>C	NP_057457.1:n.-267G>C
NM_130791.3:c.-267G>C	NP_570607.1:n.-267G>C
NR_120435.1:n.100G>C
NR_120436.1:n.100G>C