Canonical Allele Identifier: CA2673856947
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs914414351
gnomAD v4: 5-55233640-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233640C>T , CM000667.2:g.55233640C>T GRCh38
NC_000005.9:g.54529468C>T , CM000667.1:g.54529468C>T GRCh37
NC_000005.8:g.54565225C>T NCBI36
NG_034201.1:g.5078G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-117G>A ENSP00000282572.4:n.-117G>A
NM_021147.4:c.-117G>A NP_066970.3:n.-117G>A
NR_125346.1:n.78G>A
NR_125347.1:n.78G>A
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