Canonical Allele Identifier: CA2234888468
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099452G= , CM000678.2:g.78099452G= GRCh38
NC_000016.9:g.78133349G= , CM000678.1:g.78133349G= GRCh37
NC_000016.8:g.76690850G= NCBI36
NG_011698.1:g.4799G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-327G= ENSP00000485925.2:n.-327G=
ENST00000682609.1:n.1G=
ENST00000683286.1:n.1G=
ENST00000683929.1:c.-327G= ENSP00000507689.1:n.-327G=
ENST00000684070.1:n.3G=
ENST00000684381.1:n.1G=
ENST00000684452.1:n.1G=
ENST00000684632.1:n.53G=
ENST00000566780.5:c.-327G= ENSP00000457230.1:n.-327G=
ENST00000627394.2:c.-327G= ENSP00000485925.1:n.-327G=
NM_001291997.1:c.-601G= NP_001278926.1:n.-601G=
NM_016373.3:c.-327G= NP_057457.1:n.-327G=
NM_130791.3:c.-327G= NP_570607.1:n.-327G=
NR_120435.1:n.40G=
NR_120436.1:n.40G=