Canonical Allele Identifier: CA2673856978
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233658-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233658T>G , CM000667.2:g.55233658T>G GRCh38
NC_000005.9:g.54529486T>G , CM000667.1:g.54529486T>G GRCh37
NC_000005.8:g.54565243T>G NCBI36
NG_034201.1:g.5060A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-135A>C ENSP00000282572.4:n.-135A>C
NM_021147.4:c.-135A>C NP_066970.3:n.-135A>C
NR_125346.1:n.60A>C
NR_125347.1:n.60A>C
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