Canonical Allele Identifier: CA812218145
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1184820576
gnomAD v4: 5-55233045-C-T
MyVariant Identifiers: chr5:g.54528873C>T (hg19) chr5:g.55233045C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233045C>T , CM000667.2:g.55233045C>T GRCh38
NC_000005.9:g.54528873C>T , CM000667.1:g.54528873C>T GRCh37
NC_000005.8:g.54564630C>T NCBI36
NG_034201.1:g.5673G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+98G>A MANE Select ENSP00000282572.4:n.381+98G>A
ENST00000282572.4:c.381+98G>A ENSP00000282572.4:n.381+98G>A
ENST00000501463.2:c.*83G>A ENSP00000422485.1:n.*83G>A
NM_021147.4:c.381+98G>A NP_066970.3:n.381+98G>A
NR_125346.1:n.673G>A
NR_125347.1:n.580+93G>A
NM_021147.5:c.381+98G>A MANE Select NP_066970.3:n.381+98G>A
NR_125346.2:n.564G>A
NR_125347.2:n.471+93G>A
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