Canonical Allele Identifier: CA359724950
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233315C>A , CM000667.2:g.55233315C>A GRCh38
NC_000005.9:g.54529143C>A , CM000667.1:g.54529143C>A GRCh37
NC_000005.8:g.54564900C>A NCBI36
NG_034201.1:g.5403G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.209G>T MANE Select ENSP00000282572.4:p.Gly70Val
ENST00000282572.4:c.209G>T ENSP00000282572.4:p.Gly70Val
ENST00000501463.2:c.209G>T ENSP00000422485.1:p.Gly70Val
NM_021147.4:c.209G>T NP_066970.3:p.Gly70Val
NR_125346.1:n.403G>T
NR_125347.1:n.403G>T
NM_021147.5:c.209G>T MANE Select NP_066970.3:p.Gly70Val
NR_125346.2:n.294G>T
NR_125347.2:n.294G>T