Canonical Allele Identifier: CA2234888447
Gene: WWOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.78099438C= , CM000678.2:g.78099438C= GRCh38
NC_000016.9:g.78133335C= , CM000678.1:g.78133335C= GRCh37
NC_000016.8:g.76690836C= NCBI36
NG_011698.1:g.4785C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000627394.3:c.-341C= ENSP00000485925.2:n.-341C=
ENST00000683929.1:c.-341C= ENSP00000507689.1:n.-341C=
ENST00000684632.1:n.39C=
ENST00000566780.5:c.-341C= ENSP00000457230.1:n.-341C=
ENST00000627394.2:c.-341C= ENSP00000485925.1:n.-341C=
NM_001291997.1:c.-615C= NP_001278926.1:n.-615C=
NM_016373.3:c.-341C= NP_057457.1:n.-341C=
NM_130791.3:c.-341C= NP_570607.1:n.-341C=
NR_120435.1:n.26C=
NR_120436.1:n.26C=