Canonical Allele Identifier: CA3266873
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 644509
ClinVar RCV Id: RCV000798445 RCV004027958
dbSNP Id: rs748757403
ExAC: 5:54529290 T / C
gnomAD v2: 5-54529290-T-C
gnomAD v3: 5-55233462-T-C
gnomAD v4: 5-55233462-T-C
MyVariant Identifiers: chr5:g.54529290T>C (hg19) chr5:g.55233462T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233462T>C , CM000667.2:g.55233462T>C GRCh38
NC_000005.9:g.54529290T>C , CM000667.1:g.54529290T>C GRCh37
NC_000005.8:g.54565047T>C NCBI36
NG_034201.1:g.5256A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.62A>G MANE Select ENSP00000282572.4:p.Asn21Ser
ENST00000282572.4:c.62A>G ENSP00000282572.4:p.Asn21Ser
ENST00000501463.2:c.62A>G ENSP00000422485.1:p.Asn21Ser
NM_021147.4:c.62A>G NP_066970.3:p.Asn21Ser
NR_125346.1:n.256A>G
NR_125347.1:n.256A>G
NM_021147.5:c.62A>G MANE Select NP_066970.3:p.Asn21Ser
NR_125346.2:n.147A>G
NR_125347.2:n.147A>G
Search 100 bp 5'
Search 100 bp 3'