Canonical Allele Identifier: CA2234888647
Gene: WWOX HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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