Canonical Allele Identifier: CA11929324
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 1263712
ClinVar RCV Id: RCV001674706
dbSNP Id: rs231623
gnomAD v2: 5-54529458-C-G
gnomAD v3: 5-55233630-C-G
gnomAD v4: 5-55233630-C-G
MyVariant Identifiers: chr5:g.54529458C>G (hg19) chr5:g.55233630C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233630C>G , CM000667.2:g.55233630C>G GRCh38
NC_000005.9:g.54529458C>G , CM000667.1:g.54529458C>G GRCh37
NC_000005.8:g.54565215C>G NCBI36
NG_034201.1:g.5088G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-107G>C ENSP00000282572.4:n.-107G>C
NM_021147.4:c.-107G>C NP_066970.3:n.-107G>C
NR_125346.1:n.88G>C
NR_125347.1:n.88G>C
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