Canonical Allele Identifier: CA359724437
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233230G>C , CM000667.2:g.55233230G>C GRCh38
NC_000005.9:g.54529058G>C , CM000667.1:g.54529058G>C GRCh37
NC_000005.8:g.54564815G>C NCBI36
NG_034201.1:g.5488C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.294C>G MANE Select ENSP00000282572.4:p.Phe98Leu
ENST00000282572.4:c.294C>G ENSP00000282572.4:p.Phe98Leu
ENST00000501463.2:c.294C>G ENSP00000422485.1:p.Phe98Leu
NM_021147.4:c.294C>G NP_066970.3:p.Phe98Leu
NR_125346.1:n.488C>G
NR_125347.1:n.488C>G
NM_021147.5:c.294C>G MANE Select NP_066970.3:p.Phe98Leu
NR_125346.2:n.379C>G
NR_125347.2:n.379C>G