Canonical Allele Identifier: CA1547391057
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1745674671
gnomAD v4: 5-55233645-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233645G>C , CM000667.2:g.55233645G>C GRCh38
NC_000005.9:g.54529473G>C , CM000667.1:g.54529473G>C GRCh37
NC_000005.8:g.54565230G>C NCBI36
NG_034201.1:g.5073C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-122C>G ENSP00000282572.4:n.-122C>G
NM_021147.4:c.-122C>G NP_066970.3:n.-122C>G
NR_125346.1:n.73C>G
NR_125347.1:n.73C>G
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