Canonical Allele Identifier: CA559343763
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1470699772
gnomAD v2: 5-54529434-G-A
gnomAD v3: 5-55233606-G-A
gnomAD v4: 5-55233606-G-A
MyVariant Identifiers: chr5:g.54529434G>A (hg19) chr5:g.55233606G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233606G>A , CM000667.2:g.55233606G>A GRCh38
NC_000005.9:g.54529434G>A , CM000667.1:g.54529434G>A GRCh37
NC_000005.8:g.54565191G>A NCBI36
NG_034201.1:g.5112C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-83C>T MANE Select ENSP00000282572.4:n.-83C>T
ENST00000282572.4:c.-83C>T ENSP00000282572.4:n.-83C>T
NM_021147.4:c.-83C>T NP_066970.3:n.-83C>T
NR_125346.1:n.112C>T
NR_125347.1:n.112C>T
NM_021147.5:c.-83C>T MANE Select NP_066970.3:n.-83C>T
NR_125346.2:n.3C>T
NR_125347.2:n.3C>T
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