Canonical Allele Identifier: CA2673856935
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233633-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233633A>C , CM000667.2:g.55233633A>C GRCh38
NC_000005.9:g.54529461A>C , CM000667.1:g.54529461A>C GRCh37
NC_000005.8:g.54565218A>C NCBI36
NG_034201.1:g.5085T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-110T>G ENSP00000282572.4:n.-110T>G
NM_021147.4:c.-110T>G NP_066970.3:n.-110T>G
NR_125346.1:n.85T>G
NR_125347.1:n.85T>G
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