Canonical Allele Identifier: CA2673856353
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232981-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232981T>G , CM000667.2:g.55232981T>G GRCh38
NC_000005.9:g.54528809T>G , CM000667.1:g.54528809T>G GRCh37
NC_000005.8:g.54564566T>G NCBI36
NG_034201.1:g.5737A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+162A>C MANE Select ENSP00000282572.4:n.381+162A>C
ENST00000282572.4:c.381+162A>C ENSP00000282572.4:n.381+162A>C
ENST00000501463.2:c.*147A>C ENSP00000422485.1:n.*147A>C
NM_021147.4:c.381+162A>C NP_066970.3:n.381+162A>C
NR_125346.1:n.737A>C
NR_125347.1:n.580+157A>C
NR_125348.1:n.11A>C
NM_021147.5:c.381+162A>C MANE Select NP_066970.3:n.381+162A>C
NR_125346.2:n.628A>C
NR_125347.2:n.471+157A>C
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