Canonical Allele Identifier: CA1547396568
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1580411663
gnomAD v4: 5-55232965-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232965T>A , CM000667.2:g.55232965T>A GRCh38
NC_000005.9:g.54528793T>A , CM000667.1:g.54528793T>A GRCh37
NC_000005.8:g.54564550T>A NCBI36
NG_034201.1:g.5753A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+178A>T MANE Select ENSP00000282572.4:n.381+178A>T
ENST00000282572.4:c.381+178A>T ENSP00000282572.4:n.381+178A>T
ENST00000501463.2:c.*163A>T ENSP00000422485.1:n.*163A>T
NM_021147.4:c.381+178A>T NP_066970.3:n.381+178A>T
NR_125346.1:n.753A>T
NR_125347.1:n.580+173A>T
NR_125348.1:n.27A>T
NM_021147.5:c.381+178A>T MANE Select NP_066970.3:n.381+178A>T
NR_125346.2:n.644A>T
NR_125347.2:n.471+173A>T
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