Canonical Allele Identifier: CA1076233952
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs763376831
gnomAD v3: 5-55233534-G-T
gnomAD v4: 5-55233534-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233534G>T , CM000667.2:g.55233534G>T GRCh38
NC_000005.9:g.54529362G>T , CM000667.1:g.54529362G>T GRCh37
NC_000005.8:g.54565119G>T NCBI36
NG_034201.1:g.5184C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-11C>A MANE Select ENSP00000282572.4:n.-11C>A
ENST00000282572.4:c.-11C>A ENSP00000282572.4:n.-11C>A
ENST00000501463.2:c.-11C>A ENSP00000422485.1:n.-11C>A
NM_021147.4:c.-11C>A NP_066970.3:n.-11C>A
NR_125346.1:n.184C>A
NR_125347.1:n.184C>A
NM_021147.5:c.-11C>A MANE Select NP_066970.3:n.-11C>A
NR_125346.2:n.75C>A
NR_125347.2:n.75C>A
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