Canonical Allele Identifier: CA2673856450
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233056-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233056G>T , CM000667.2:g.55233056G>T GRCh38
NC_000005.9:g.54528884G>T , CM000667.1:g.54528884G>T GRCh37
NC_000005.8:g.54564641G>T NCBI36
NG_034201.1:g.5662C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+87C>A MANE Select ENSP00000282572.4:n.381+87C>A
ENST00000282572.4:c.381+87C>A ENSP00000282572.4:n.381+87C>A
ENST00000501463.2:c.*72C>A ENSP00000422485.1:n.*72C>A
NM_021147.4:c.381+87C>A NP_066970.3:n.381+87C>A
NR_125346.1:n.662C>A
NR_125347.1:n.580+82C>A
NM_021147.5:c.381+87C>A MANE Select NP_066970.3:n.381+87C>A
NR_125346.2:n.553C>A
NR_125347.2:n.471+82C>A
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