Canonical Allele Identifier: CA359721154
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs150766906
MyVariant Identifiers: chr5:g.54527471G>C (hg19) chr5:g.55231643G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55231643G>C , CM000667.2:g.55231643G>C GRCh38
NC_000005.9:g.54527471G>C , CM000667.1:g.54527471G>C GRCh37
NC_000005.8:g.54563228G>C NCBI36
NG_034201.1:g.7075C>G
NG_051620.1:g.673C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.785C>G MANE Select ENSP00000282572.4:p.Ala262Gly
ENST00000282572.4:c.785C>G ENSP00000282572.4:p.Ala262Gly
ENST00000501463.2:c.*765C>G ENSP00000422485.1:n.*765C>G
NM_021147.4:c.785C>G NP_066970.3:p.Ala262Gly
NR_125346.1:n.1355C>G
NR_125347.1:n.984C>G
NR_125348.1:n.849C>G
NM_021147.5:c.785C>G MANE Select NP_066970.3:p.Ala262Gly
NR_125346.2:n.1246C>G
NR_125347.2:n.875C>G
Search 100 bp 5'
Search 100 bp 3'