Canonical Allele Identifier: CA2673856976
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233657-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233657C>A , CM000667.2:g.55233657C>A GRCh38
NC_000005.9:g.54529485C>A , CM000667.1:g.54529485C>A GRCh37
NC_000005.8:g.54565242C>A NCBI36
NG_034201.1:g.5061G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-134G>T ENSP00000282572.4:n.-134G>T
NM_021147.4:c.-134G>T NP_066970.3:n.-134G>T
NR_125346.1:n.61G>T
NR_125347.1:n.61G>T
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