Canonical Allele Identifier: CA2673856962
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233652_55233654del , CM000667.2:g.55233652_55233654del GRCh38
NC_000005.9:g.54529480_54529482del , CM000667.1:g.54529480_54529482del GRCh37
NC_000005.8:g.54565237_54565239del NCBI36
NG_034201.1:g.5066_5068del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-129_-127del ENSP00000282572.4:n.-129_-127del
NM_021147.4:c.-129_-127del NP_066970.3:n.-129_-127del
NR_125346.1:n.66_68del
NR_125347.1:n.66_68del