Canonical Allele Identifier: CA2673856945
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233639-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233639C>A , CM000667.2:g.55233639C>A GRCh38
NC_000005.9:g.54529467C>A , CM000667.1:g.54529467C>A GRCh37
NC_000005.8:g.54565224C>A NCBI36
NG_034201.1:g.5079G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-116G>T ENSP00000282572.4:n.-116G>T
NM_021147.4:c.-116G>T NP_066970.3:n.-116G>T
NR_125346.1:n.79G>T
NR_125347.1:n.79G>T
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