Canonical Allele Identifier: CA359725265
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233358C>G , CM000667.2:g.55233358C>G GRCh38
NC_000005.9:g.54529186C>G , CM000667.1:g.54529186C>G GRCh37
NC_000005.8:g.54564943C>G NCBI36
NG_034201.1:g.5360G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.166G>C MANE Select ENSP00000282572.4:p.Gly56Arg
ENST00000282572.4:c.166G>C ENSP00000282572.4:p.Gly56Arg
ENST00000501463.2:c.166G>C ENSP00000422485.1:p.Gly56Arg
NM_021147.4:c.166G>C NP_066970.3:p.Gly56Arg
NR_125346.1:n.360G>C
NR_125347.1:n.360G>C
NM_021147.5:c.166G>C MANE Select NP_066970.3:p.Gly56Arg
NR_125346.2:n.251G>C
NR_125347.2:n.251G>C