Canonical Allele Identifier: CA2673856930
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233629-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233629T>A , CM000667.2:g.55233629T>A GRCh38
NC_000005.9:g.54529457T>A , CM000667.1:g.54529457T>A GRCh37
NC_000005.8:g.54565214T>A NCBI36
NG_034201.1:g.5089A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-106A>T ENSP00000282572.4:n.-106A>T
NM_021147.4:c.-106A>T NP_066970.3:n.-106A>T
NR_125346.1:n.89A>T
NR_125347.1:n.89A>T
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