Canonical Allele Identifier: CA118945813
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs968323002
gnomAD v3: 5-55233675-C-G
gnomAD v4: 5-55233675-C-G
MyVariant Identifiers: chr5:g.54529503C>G (hg19) chr5:g.55233675C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233675C>G , CM000667.2:g.55233675C>G GRCh38
NC_000005.9:g.54529503C>G , CM000667.1:g.54529503C>G GRCh37
NC_000005.8:g.54565260C>G NCBI36
NG_034201.1:g.5043G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-152G>C ENSP00000282572.4:n.-152G>C
NM_021147.4:c.-152G>C NP_066970.3:n.-152G>C
NR_125346.1:n.43G>C
NR_125347.1:n.43G>C
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