Canonical Allele Identifier: CA2673857010
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233684-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233684T>C , CM000667.2:g.55233684T>C GRCh38
NC_000005.9:g.54529512T>C , CM000667.1:g.54529512T>C GRCh37
NC_000005.8:g.54565269T>C NCBI36
NG_034201.1:g.5034A>G

Transcript Alleles

HGVS Amino-acid Change
NM_021147.4:c.-161A>G NP_066970.3:n.-161A>G
NR_125346.1:n.34A>G
NR_125347.1:n.34A>G
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