Canonical Allele Identifier: CA2673856981
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233660-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233660C>T , CM000667.2:g.55233660C>T GRCh38
NC_000005.9:g.54529488C>T , CM000667.1:g.54529488C>T GRCh37
NC_000005.8:g.54565245C>T NCBI36
NG_034201.1:g.5058G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-137G>A ENSP00000282572.4:n.-137G>A
NM_021147.4:c.-137G>A NP_066970.3:n.-137G>A
NR_125346.1:n.58G>A
NR_125347.1:n.58G>A
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