Canonical Allele Identifier: CA2673856990
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233669-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233669C>A , CM000667.2:g.55233669C>A GRCh38
NC_000005.9:g.54529497C>A , CM000667.1:g.54529497C>A GRCh37
NC_000005.8:g.54565254C>A NCBI36
NG_034201.1:g.5049G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-146G>T ENSP00000282572.4:n.-146G>T
NM_021147.4:c.-146G>T NP_066970.3:n.-146G>T
NR_125346.1:n.49G>T
NR_125347.1:n.49G>T
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