Canonical Allele Identifier: CA118944660
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs568442022
MyVariant Identifiers: chr5:g.54528767T>G (hg19) chr5:g.55232939T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232939T>G , CM000667.2:g.55232939T>G GRCh38
NC_000005.9:g.54528767T>G , CM000667.1:g.54528767T>G GRCh37
NC_000005.8:g.54564524T>G NCBI36
NG_034201.1:g.5779A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+204A>C MANE Select ENSP00000282572.4:n.381+204A>C
ENST00000282572.4:c.381+204A>C ENSP00000282572.4:n.381+204A>C
ENST00000501463.2:c.*189A>C ENSP00000422485.1:n.*189A>C
NM_021147.4:c.381+204A>C NP_066970.3:n.381+204A>C
NR_125346.1:n.779A>C
NR_125347.1:n.580+199A>C
NR_125348.1:n.53A>C
NM_021147.5:c.381+204A>C MANE Select NP_066970.3:n.381+204A>C
NR_125346.2:n.670A>C
NR_125347.2:n.471+199A>C
Search 100 bp 5'
Search 100 bp 3'