Canonical Allele Identifier: CA444397267
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 2769081
ClinVar RCV Id: RCV003538224
gnomAD v4: 5-55233371-G-C
MyVariant Identifiers: chr5:g.54529199G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233371G>C , CM000667.2:g.55233371G>C GRCh38
NC_000005.9:g.54529199G>C , CM000667.1:g.54529199G>C GRCh37
NC_000005.8:g.54564956G>C NCBI36
NG_034201.1:g.5347C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.153C>G MANE Select ENSP00000282572.4:p.Leu51=
ENST00000282572.4:c.153C>G ENSP00000282572.4:p.Leu51=
ENST00000501463.2:c.153C>G ENSP00000422485.1:p.Leu51=
NM_021147.4:c.153C>G NP_066970.3:p.Leu51=
NR_125346.1:n.347C>G
NR_125347.1:n.347C>G
NM_021147.5:c.153C>G MANE Select NP_066970.3:p.Leu51=
NR_125346.2:n.238C>G
NR_125347.2:n.238C>G
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