Canonical Allele Identifier: CA559800459
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1432639315
gnomAD v2: 5-54528857-G-A
gnomAD v3: 5-55233029-G-A
gnomAD v4: 5-55233029-G-A
MyVariant Identifiers: chr5:g.54528857G>A (hg19) chr5:g.55233029G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233029G>A , CM000667.2:g.55233029G>A GRCh38
NC_000005.9:g.54528857G>A , CM000667.1:g.54528857G>A GRCh37
NC_000005.8:g.54564614G>A NCBI36
NG_034201.1:g.5689C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+114C>T MANE Select ENSP00000282572.4:n.381+114C>T
ENST00000282572.4:c.381+114C>T ENSP00000282572.4:n.381+114C>T
ENST00000501463.2:c.*99C>T ENSP00000422485.1:n.*99C>T
NM_021147.4:c.381+114C>T NP_066970.3:n.381+114C>T
NR_125346.1:n.689C>T
NR_125347.1:n.580+109C>T
NM_021147.5:c.381+114C>T MANE Select NP_066970.3:n.381+114C>T
NR_125346.2:n.580C>T
NR_125347.2:n.471+109C>T
Search 100 bp 5'
Search 100 bp 3'