Canonical Allele Identifier: CA2673856977
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233658-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233658T>A , CM000667.2:g.55233658T>A GRCh38
NC_000005.9:g.54529486T>A , CM000667.1:g.54529486T>A GRCh37
NC_000005.8:g.54565243T>A NCBI36
NG_034201.1:g.5060A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-135A>T ENSP00000282572.4:n.-135A>T
NM_021147.4:c.-135A>T NP_066970.3:n.-135A>T
NR_125346.1:n.60A>T
NR_125347.1:n.60A>T