Canonical Allele Identifier: CA2673856987
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233667-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233667C>A , CM000667.2:g.55233667C>A GRCh38
NC_000005.9:g.54529495C>A , CM000667.1:g.54529495C>A GRCh37
NC_000005.8:g.54565252C>A NCBI36
NG_034201.1:g.5051G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-144G>T ENSP00000282572.4:n.-144G>T
NM_021147.4:c.-144G>T NP_066970.3:n.-144G>T
NR_125346.1:n.51G>T
NR_125347.1:n.51G>T
Search 100 bp 5'
Search 100 bp 3'