Canonical Allele Identifier: CA1547391071
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233654T= , CM000667.2:g.55233654T= GRCh38
NC_000005.9:g.54529482T= , CM000667.1:g.54529482T= GRCh37
NC_000005.8:g.54565239T= NCBI36
NG_034201.1:g.5064A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-131A= ENSP00000282572.4:n.-131A=
NM_021147.4:c.-131A= NP_066970.3:n.-131A=
NR_125346.1:n.64A=
NR_125347.1:n.64A=