Canonical Allele Identifier: CA2554052533
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233675C>A , CM000667.2:g.55233675C>A GRCh38
NC_000005.9:g.54529503C>A , CM000667.1:g.54529503C>A GRCh37
NC_000005.8:g.54565260C>A NCBI36
NG_034201.1:g.5043G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-152G>T ENSP00000282572.4:n.-152G>T
NM_021147.4:c.-152G>T NP_066970.3:n.-152G>T
NR_125346.1:n.43G>T
NR_125347.1:n.43G>T
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