Canonical Allele Identifier: CA1547390983
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233599G= , CM000667.2:g.55233599G= GRCh38
NC_000005.9:g.54529427G= , CM000667.1:g.54529427G= GRCh37
NC_000005.8:g.54565184G= NCBI36
NG_034201.1:g.5119C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-76C= MANE Select ENSP00000282572.4:n.-76C=
ENST00000282572.4:c.-76C= ENSP00000282572.4:n.-76C=
NM_021147.4:c.-76C= NP_066970.3:n.-76C=
NR_125346.1:n.119C=
NR_125347.1:n.119C=
NM_021147.5:c.-76C= MANE Select NP_066970.3:n.-76C=
NR_125346.2:n.10C=
NR_125347.2:n.10C=
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