Canonical Allele Identifier: CA2234888438

Gene: WWOX

Linked Data

• dbSNP Id: rs1055930883

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099429G>C , CM000678.2:g.78099429G>C	GRCh38
NC_000016.9:g.78133326G>C , CM000678.1:g.78133326G>C	GRCh37
NC_000016.8:g.76690827G>C	NCBI36
NG_011698.1:g.4776G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-350G>C	ENSP00000485925.2:n.-350G>C
ENST00000683929.1:c.-350G>C	ENSP00000507689.1:n.-350G>C
ENST00000684632.1:n.30G>C
ENST00000566780.5:c.-350G>C	ENSP00000457230.1:n.-350G>C
NM_001291997.1:c.-624G>C	NP_001278926.1:n.-624G>C
NM_016373.3:c.-350G>C	NP_057457.1:n.-350G>C
NM_130791.3:c.-350G>C	NP_570607.1:n.-350G>C
NR_120435.1:n.17G>C
NR_120436.1:n.17G>C