Canonical Allele Identifier: CA559343687
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1309074432
gnomAD v2: 5-54528754-G-A
gnomAD v3: 5-55232926-G-A
gnomAD v4: 5-55232926-G-A
MyVariant Identifiers: chr5:g.54528754G>A (hg19) chr5:g.55232926G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232926G>A , CM000667.2:g.55232926G>A GRCh38
NC_000005.9:g.54528754G>A , CM000667.1:g.54528754G>A GRCh37
NC_000005.8:g.54564511G>A NCBI36
NG_034201.1:g.5792C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+217C>T MANE Select ENSP00000282572.4:n.381+217C>T
ENST00000282572.4:c.381+217C>T ENSP00000282572.4:n.381+217C>T
ENST00000501463.2:c.*202C>T ENSP00000422485.1:n.*202C>T
NM_021147.4:c.381+217C>T NP_066970.3:n.381+217C>T
NR_125346.1:n.792C>T
NR_125347.1:n.580+212C>T
NR_125348.1:n.66C>T
NM_021147.5:c.381+217C>T MANE Select NP_066970.3:n.381+217C>T
NR_125346.2:n.683C>T
NR_125347.2:n.471+212C>T
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