Canonical Allele Identifier: CA1547391018
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1157688614
gnomAD v4: 5-55233629-T-C
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Genomic Alleles

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

Transcript Alleles

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