Canonical Allele Identifier: CA2673856347
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232976-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232976T>G , CM000667.2:g.55232976T>G GRCh38
NC_000005.9:g.54528804T>G , CM000667.1:g.54528804T>G GRCh37
NC_000005.8:g.54564561T>G NCBI36
NG_034201.1:g.5742A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+167A>C MANE Select ENSP00000282572.4:n.381+167A>C
ENST00000282572.4:c.381+167A>C ENSP00000282572.4:n.381+167A>C
ENST00000501463.2:c.*152A>C ENSP00000422485.1:n.*152A>C
NM_021147.4:c.381+167A>C NP_066970.3:n.381+167A>C
NR_125346.1:n.742A>C
NR_125347.1:n.580+162A>C
NR_125348.1:n.16A>C
NM_021147.5:c.381+167A>C MANE Select NP_066970.3:n.381+167A>C
NR_125346.2:n.633A>C
NR_125347.2:n.471+162A>C
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