Canonical Allele Identifier: CA2673856918
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233620-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233620C>A , CM000667.2:g.55233620C>A GRCh38
NC_000005.9:g.54529448C>A , CM000667.1:g.54529448C>A GRCh37
NC_000005.8:g.54565205C>A NCBI36
NG_034201.1:g.5098G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-97G>T ENSP00000282572.4:n.-97G>T
NM_021147.4:c.-97G>T NP_066970.3:n.-97G>T
NR_125346.1:n.98G>T
NR_125347.1:n.98G>T