Canonical Allele Identifier: CA2673856442
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233051-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233051C>G , CM000667.2:g.55233051C>G GRCh38
NC_000005.9:g.54528879C>G , CM000667.1:g.54528879C>G GRCh37
NC_000005.8:g.54564636C>G NCBI36
NG_034201.1:g.5667G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+92G>C MANE Select ENSP00000282572.4:n.381+92G>C
ENST00000282572.4:c.381+92G>C ENSP00000282572.4:n.381+92G>C
ENST00000501463.2:c.*77G>C ENSP00000422485.1:n.*77G>C
NM_021147.4:c.381+92G>C NP_066970.3:n.381+92G>C
NR_125346.1:n.667G>C
NR_125347.1:n.580+87G>C
NM_021147.5:c.381+92G>C MANE Select NP_066970.3:n.381+92G>C
NR_125346.2:n.558G>C
NR_125347.2:n.471+87G>C
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