Canonical Allele Identifier: CA2234888649

Gene: WWOX

Linked Data

• dbSNP Id: rs1597188916

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099553A>C , CM000678.2:g.78099553A>C	GRCh38
NC_000016.9:g.78133450A>C , CM000678.1:g.78133450A>C	GRCh37
NC_000016.8:g.76690951A>C	NCBI36
NG_011698.1:g.4900A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-226A>C	ENSP00000485925.2:n.-226A>C
ENST00000682609.1:n.102A>C
ENST00000683286.1:n.102A>C
ENST00000683929.1:c.-226A>C	ENSP00000507689.1:n.-226A>C
ENST00000684070.1:n.104A>C
ENST00000684381.1:n.102A>C
ENST00000684452.1:n.102A>C
ENST00000684632.1:n.154A>C
ENST00000566780.5:c.-226A>C	ENSP00000457230.1:n.-226A>C
ENST00000627394.2:c.-226A>C	ENSP00000485925.1:n.-226A>C
NM_001291997.1:c.-500A>C	NP_001278926.1:n.-500A>C
NM_016373.3:c.-226A>C	NP_057457.1:n.-226A>C
NM_130791.3:c.-226A>C	NP_570607.1:n.-226A>C
NR_120435.1:n.141A>C
NR_120436.1:n.141A>C