Canonical Allele Identifier: CA3266852
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs781019205
ExAC: 5:54529215 A / C
gnomAD v2: 5-54529215-A-C
gnomAD v4: 5-55233387-A-C
MyVariant Identifiers: chr5:g.54529215A>C (hg19) chr5:g.55233387A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233387A>C , CM000667.2:g.55233387A>C GRCh38
NC_000005.9:g.54529215A>C , CM000667.1:g.54529215A>C GRCh37
NC_000005.8:g.54564972A>C NCBI36
NG_034201.1:g.5331T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.137T>G MANE Select ENSP00000282572.4:p.Leu46Arg
ENST00000282572.4:c.137T>G ENSP00000282572.4:p.Leu46Arg
ENST00000501463.2:c.137T>G ENSP00000422485.1:p.Leu46Arg
NM_021147.4:c.137T>G NP_066970.3:p.Leu46Arg
NR_125346.1:n.331T>G
NR_125347.1:n.331T>G
NM_021147.5:c.137T>G MANE Select NP_066970.3:p.Leu46Arg
NR_125346.2:n.222T>G
NR_125347.2:n.222T>G
Search 100 bp 5'
Search 100 bp 3'