Canonical Allele Identifier: CA2673856311
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232935-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232935C>G , CM000667.2:g.55232935C>G GRCh38
NC_000005.9:g.54528763C>G , CM000667.1:g.54528763C>G GRCh37
NC_000005.8:g.54564520C>G NCBI36
NG_034201.1:g.5783G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+208G>C MANE Select ENSP00000282572.4:n.381+208G>C
ENST00000282572.4:c.381+208G>C ENSP00000282572.4:n.381+208G>C
ENST00000501463.2:c.*193G>C ENSP00000422485.1:n.*193G>C
NM_021147.4:c.381+208G>C NP_066970.3:n.381+208G>C
NR_125346.1:n.783G>C
NR_125347.1:n.580+203G>C
NR_125348.1:n.57G>C
NM_021147.5:c.381+208G>C MANE Select NP_066970.3:n.381+208G>C
NR_125346.2:n.674G>C
NR_125347.2:n.471+203G>C
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