Canonical Allele Identifier: CA559800458
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1468761340
gnomAD v2: 5-54528833-G-T
gnomAD v3: 5-55233005-G-T
gnomAD v4: 5-55233005-G-T
MyVariant Identifiers: chr5:g.54528833G>T (hg19) chr5:g.55233005G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233005G>T , CM000667.2:g.55233005G>T GRCh38
NC_000005.9:g.54528833G>T , CM000667.1:g.54528833G>T GRCh37
NC_000005.8:g.54564590G>T NCBI36
NG_034201.1:g.5713C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+138C>A MANE Select ENSP00000282572.4:n.381+138C>A
ENST00000282572.4:c.381+138C>A ENSP00000282572.4:n.381+138C>A
ENST00000501463.2:c.*123C>A ENSP00000422485.1:n.*123C>A
NM_021147.4:c.381+138C>A NP_066970.3:n.381+138C>A
NR_125346.1:n.713C>A
NR_125347.1:n.580+133C>A
NM_021147.5:c.381+138C>A MANE Select NP_066970.3:n.381+138C>A
NR_125346.2:n.604C>A
NR_125347.2:n.471+133C>A
Search 100 bp 5'
Search 100 bp 3'