Canonical Allele Identifier: CA1547391077
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233659A= , CM000667.2:g.55233659A= GRCh38
NC_000005.9:g.54529487A= , CM000667.1:g.54529487A= GRCh37
NC_000005.8:g.54565244A= NCBI36
NG_034201.1:g.5059T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-136T= ENSP00000282572.4:n.-136T=
NM_021147.4:c.-136T= NP_066970.3:n.-136T=
NR_125346.1:n.59T=
NR_125347.1:n.59T=