Canonical Allele Identifier: CA2673856941
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233637-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233637A>G , CM000667.2:g.55233637A>G GRCh38
NC_000005.9:g.54529465A>G , CM000667.1:g.54529465A>G GRCh37
NC_000005.8:g.54565222A>G NCBI36
NG_034201.1:g.5081T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-114T>C ENSP00000282572.4:n.-114T>C
NM_021147.4:c.-114T>C NP_066970.3:n.-114T>C
NR_125346.1:n.81T>C
NR_125347.1:n.81T>C