Canonical Allele Identifier: CA2673856342
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232971-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232971A>T , CM000667.2:g.55232971A>T GRCh38
NC_000005.9:g.54528799A>T , CM000667.1:g.54528799A>T GRCh37
NC_000005.8:g.54564556A>T NCBI36
NG_034201.1:g.5747T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+172T>A MANE Select ENSP00000282572.4:n.381+172T>A
ENST00000282572.4:c.381+172T>A ENSP00000282572.4:n.381+172T>A
ENST00000501463.2:c.*157T>A ENSP00000422485.1:n.*157T>A
NM_021147.4:c.381+172T>A NP_066970.3:n.381+172T>A
NR_125346.1:n.747T>A
NR_125347.1:n.580+167T>A
NR_125348.1:n.21T>A
NM_021147.5:c.381+172T>A MANE Select NP_066970.3:n.381+172T>A
NR_125346.2:n.638T>A
NR_125347.2:n.471+167T>A
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