Canonical Allele Identifier: CA118944825
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 1195007
ClinVar RCV Id: RCV001557931
dbSNP Id: rs76821675
gnomAD v2: 5-54528905-G-A
gnomAD v3: 5-55233077-G-A
gnomAD v4: 5-55233077-G-A
MyVariant Identifiers: chr5:g.54528905G>A (hg19) chr5:g.55233077G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233077G>A , CM000667.2:g.55233077G>A GRCh38
NC_000005.9:g.54528905G>A , CM000667.1:g.54528905G>A GRCh37
NC_000005.8:g.54564662G>A NCBI36
NG_034201.1:g.5641C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+66C>T MANE Select ENSP00000282572.4:n.381+66C>T
ENST00000282572.4:c.381+66C>T ENSP00000282572.4:n.381+66C>T
ENST00000501463.2:c.*51C>T ENSP00000422485.1:n.*51C>T
NM_021147.4:c.381+66C>T NP_066970.3:n.381+66C>T
NR_125346.1:n.641C>T
NR_125347.1:n.580+61C>T
NM_021147.5:c.381+66C>T MANE Select NP_066970.3:n.381+66C>T
NR_125346.2:n.532C>T
NR_125347.2:n.471+61C>T
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