Canonical Allele Identifier: CA3266885
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs763376831
gnomAD v2: 5-54529362-G-A
gnomAD v4: 5-55233534-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233534G>A , CM000667.2:g.55233534G>A GRCh38
NC_000005.9:g.54529362G>A , CM000667.1:g.54529362G>A GRCh37
NC_000005.8:g.54565119G>A NCBI36
NG_034201.1:g.5184C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-11C>T MANE Select ENSP00000282572.4:n.-11C>T
ENST00000282572.4:c.-11C>T ENSP00000282572.4:n.-11C>T
ENST00000501463.2:c.-11C>T ENSP00000422485.1:n.-11C>T
NM_021147.4:c.-11C>T NP_066970.3:n.-11C>T
NR_125346.1:n.184C>T
NR_125347.1:n.184C>T
NM_021147.5:c.-11C>T MANE Select NP_066970.3:n.-11C>T
NR_125346.2:n.75C>T
NR_125347.2:n.75C>T