Canonical Allele Identifier: CA2673856917
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233619-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233619G>A , CM000667.2:g.55233619G>A GRCh38
NC_000005.9:g.54529447G>A , CM000667.1:g.54529447G>A GRCh37
NC_000005.8:g.54565204G>A NCBI36
NG_034201.1:g.5099C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-96C>T ENSP00000282572.4:n.-96C>T
NM_021147.4:c.-96C>T NP_066970.3:n.-96C>T
NR_125346.1:n.99C>T
NR_125347.1:n.99C>T
Search 100 bp 5'
Search 100 bp 3'