Canonical Allele Identifier: CA2551697965
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233643-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233643C>A , CM000667.2:g.55233643C>A GRCh38
NC_000005.9:g.54529471C>A , CM000667.1:g.54529471C>A GRCh37
NC_000005.8:g.54565228C>A NCBI36
NG_034201.1:g.5075G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-120G>T ENSP00000282572.4:n.-120G>T
NM_021147.4:c.-120G>T NP_066970.3:n.-120G>T
NR_125346.1:n.75G>T
NR_125347.1:n.75G>T