Canonical Allele Identifier: CA2673856974
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233655-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233655C>T , CM000667.2:g.55233655C>T GRCh38
NC_000005.9:g.54529483C>T , CM000667.1:g.54529483C>T GRCh37
NC_000005.8:g.54565240C>T NCBI36
NG_034201.1:g.5063G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-132G>A ENSP00000282572.4:n.-132G>A
NM_021147.4:c.-132G>A NP_066970.3:n.-132G>A
NR_125346.1:n.63G>A
NR_125347.1:n.63G>A
Search 100 bp 5'
Search 100 bp 3'