Canonical Allele Identifier: CA2673856908
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233610-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233610G>T , CM000667.2:g.55233610G>T GRCh38
NC_000005.9:g.54529438G>T , CM000667.1:g.54529438G>T GRCh37
NC_000005.8:g.54565195G>T NCBI36
NG_034201.1:g.5108C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-87C>A ENSP00000282572.4:n.-87C>A
NM_021147.4:c.-87C>A NP_066970.3:n.-87C>A
NR_125346.1:n.108C>A
NR_125347.1:n.108C>A