Canonical Allele Identifier: CA1547390984
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1745672131
gnomAD v4: 5-55233599-G-T
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Genomic Alleles

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

Transcript Alleles

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