Canonical Allele Identifier: CA118945410
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1054125362
gnomAD v3: 5-55233415-G-A
gnomAD v4: 5-55233415-G-A
MyVariant Identifiers: chr5:g.54529243G>A (hg19) chr5:g.55233415G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233415G>A , CM000667.2:g.55233415G>A GRCh38
NC_000005.9:g.54529243G>A , CM000667.1:g.54529243G>A GRCh37
NC_000005.8:g.54565000G>A NCBI36
NG_034201.1:g.5303C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.109C>T MANE Select ENSP00000282572.4:p.Leu37Phe
ENST00000282572.4:c.109C>T ENSP00000282572.4:p.Leu37Phe
ENST00000501463.2:c.109C>T ENSP00000422485.1:p.Leu37Phe
NM_021147.4:c.109C>T NP_066970.3:p.Leu37Phe
NR_125346.1:n.303C>T
NR_125347.1:n.303C>T
NM_021147.5:c.109C>T MANE Select NP_066970.3:p.Leu37Phe
NR_125346.2:n.194C>T
NR_125347.2:n.194C>T
Search 100 bp 5'
Search 100 bp 3'