Canonical Allele Identifier: CA1547391119
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233692G= , CM000667.2:g.55233692G= GRCh38
NC_000005.9:g.54529520G= , CM000667.1:g.54529520G= GRCh37
NC_000005.8:g.54565277G= NCBI36
NG_034201.1:g.5026C=

Transcript Alleles

HGVS Amino-acid Change
NM_021147.4:c.-169C= NP_066970.3:n.-169C=
NR_125346.1:n.26C=
NR_125347.1:n.26C=