Canonical Allele Identifier: CA2673856372
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232992-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232992A>G , CM000667.2:g.55232992A>G GRCh38
NC_000005.9:g.54528820A>G , CM000667.1:g.54528820A>G GRCh37
NC_000005.8:g.54564577A>G NCBI36
NG_034201.1:g.5726T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+151T>C MANE Select ENSP00000282572.4:n.381+151T>C
ENST00000282572.4:c.381+151T>C ENSP00000282572.4:n.381+151T>C
ENST00000501463.2:c.*136T>C ENSP00000422485.1:n.*136T>C
NM_021147.4:c.381+151T>C NP_066970.3:n.381+151T>C
NR_125346.1:n.726T>C
NR_125347.1:n.580+146T>C
NM_021147.5:c.381+151T>C MANE Select NP_066970.3:n.381+151T>C
NR_125346.2:n.617T>C
NR_125347.2:n.471+146T>C
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