Canonical Allele Identifier: CA1547391017
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233629T= , CM000667.2:g.55233629T= GRCh38
NC_000005.9:g.54529457T= , CM000667.1:g.54529457T= GRCh37
NC_000005.8:g.54565214T= NCBI36
NG_034201.1:g.5089A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-106A= ENSP00000282572.4:n.-106A=
NM_021147.4:c.-106A= NP_066970.3:n.-106A=
NR_125346.1:n.89A=
NR_125347.1:n.89A=