Canonical Allele Identifier: CA2673857001
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233678-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233678A>C , CM000667.2:g.55233678A>C GRCh38
NC_000005.9:g.54529506A>C , CM000667.1:g.54529506A>C GRCh37
NC_000005.8:g.54565263A>C NCBI36
NG_034201.1:g.5040T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-155T>G ENSP00000282572.4:n.-155T>G
NM_021147.4:c.-155T>G NP_066970.3:n.-155T>G
NR_125346.1:n.40T>G
NR_125347.1:n.40T>G
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