Canonical Allele Identifier: CA1547391114
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1745676685

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233692_55233699del , CM000667.2:g.55233692_55233699del GRCh38
NC_000005.9:g.54529520_54529527del , CM000667.1:g.54529520_54529527del GRCh37
NC_000005.8:g.54565277_54565284del NCBI36
NG_034201.1:g.5021_5028del

Transcript Alleles

HGVS Amino-acid Change
NM_021147.4:c.-174_-167del NP_066970.3:n.-174_-167del
NR_125346.1:n.21_28del
NR_125347.1:n.21_28del