Canonical Allele Identifier: CA2673856443
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233051-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233051C>A , CM000667.2:g.55233051C>A GRCh38
NC_000005.9:g.54528879C>A , CM000667.1:g.54528879C>A GRCh37
NC_000005.8:g.54564636C>A NCBI36
NG_034201.1:g.5667G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+92G>T MANE Select ENSP00000282572.4:n.381+92G>T
ENST00000282572.4:c.381+92G>T ENSP00000282572.4:n.381+92G>T
ENST00000501463.2:c.*77G>T ENSP00000422485.1:n.*77G>T
NM_021147.4:c.381+92G>T NP_066970.3:n.381+92G>T
NR_125346.1:n.667G>T
NR_125347.1:n.580+87G>T
NM_021147.5:c.381+92G>T MANE Select NP_066970.3:n.381+92G>T
NR_125346.2:n.558G>T
NR_125347.2:n.471+87G>T
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