Canonical Allele Identifier: CA1547391116
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233690C= , CM000667.2:g.55233690C= GRCh38
NC_000005.9:g.54529518C= , CM000667.1:g.54529518C= GRCh37
NC_000005.8:g.54565275C= NCBI36
NG_034201.1:g.5028G=

Transcript Alleles

HGVS Amino-acid Change
NM_021147.4:c.-167G= NP_066970.3:n.-167G=
NR_125346.1:n.28G=
NR_125347.1:n.28G=