Canonical Allele Identifier: CA1547391088
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1745675514

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233669del , CM000667.2:g.55233669del GRCh38
NC_000005.9:g.54529497del , CM000667.1:g.54529497del GRCh37
NC_000005.8:g.54565254del NCBI36
NG_034201.1:g.5053del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-142del ENSP00000282572.4:n.-142del
NM_021147.4:c.-142del NP_066970.3:n.-142del
NR_125346.1:n.53del
NR_125347.1:n.53del