Canonical Allele Identifier: CA359724786
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1168699685
gnomAD v2: 5-54529120-G-A
gnomAD v4: 5-55233292-G-A
MyVariant Identifiers: chr5:g.54529120G>A (hg19) chr5:g.55233292G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233292G>A , CM000667.2:g.55233292G>A GRCh38
NC_000005.9:g.54529120G>A , CM000667.1:g.54529120G>A GRCh37
NC_000005.8:g.54564877G>A NCBI36
NG_034201.1:g.5426C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.232C>T MANE Select ENSP00000282572.4:p.Arg78Trp
ENST00000282572.4:c.232C>T ENSP00000282572.4:p.Arg78Trp
ENST00000501463.2:c.232C>T ENSP00000422485.1:p.Arg78Trp
NM_021147.4:c.232C>T NP_066970.3:p.Arg78Trp
NR_125346.1:n.426C>T
NR_125347.1:n.426C>T
NM_021147.5:c.232C>T MANE Select NP_066970.3:p.Arg78Trp
NR_125346.2:n.317C>T
NR_125347.2:n.317C>T
Search 100 bp 5'
Search 100 bp 3'