Canonical Allele Identifier: CA559343765
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1157688614
gnomAD v2: 5-54529457-T-G
gnomAD v3: 5-55233629-T-G
gnomAD v4: 5-55233629-T-G
MyVariant Identifiers: chr5:g.54529457T>G (hg19) chr5:g.55233629T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233629T>G , CM000667.2:g.55233629T>G GRCh38
NC_000005.9:g.54529457T>G , CM000667.1:g.54529457T>G GRCh37
NC_000005.8:g.54565214T>G NCBI36
NG_034201.1:g.5089A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-106A>C ENSP00000282572.4:n.-106A>C
NM_021147.4:c.-106A>C NP_066970.3:n.-106A>C
NR_125346.1:n.89A>C
NR_125347.1:n.89A>C
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