Canonical Allele Identifier: CA1547390999
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233611G= , CM000667.2:g.55233611G= GRCh38
NC_000005.9:g.54529439G= , CM000667.1:g.54529439G= GRCh37
NC_000005.8:g.54565196G= NCBI36
NG_034201.1:g.5107C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-88C= ENSP00000282572.4:n.-88C=
NM_021147.4:c.-88C= NP_066970.3:n.-88C=
NR_125346.1:n.107C=
NR_125347.1:n.107C=