Canonical Allele Identifier: CA2578309942
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233068-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233068G>C , CM000667.2:g.55233068G>C GRCh38
NC_000005.9:g.54528896G>C , CM000667.1:g.54528896G>C GRCh37
NC_000005.8:g.54564653G>C NCBI36
NG_034201.1:g.5650C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+75C>G MANE Select ENSP00000282572.4:n.381+75C>G
ENST00000282572.4:c.381+75C>G ENSP00000282572.4:n.381+75C>G
ENST00000501463.2:c.*60C>G ENSP00000422485.1:n.*60C>G
NM_021147.4:c.381+75C>G NP_066970.3:n.381+75C>G
NR_125346.1:n.650C>G
NR_125347.1:n.580+70C>G
NM_021147.5:c.381+75C>G MANE Select NP_066970.3:n.381+75C>G
NR_125346.2:n.541C>G
NR_125347.2:n.471+70C>G
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