Canonical Allele Identifier: CA2673856965
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233657_55233658del , CM000667.2:g.55233657_55233658del GRCh38
NC_000005.9:g.54529485_54529486del , CM000667.1:g.54529485_54529486del GRCh37
NC_000005.8:g.54565242_54565243del NCBI36
NG_034201.1:g.5065_5066del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-130_-129del ENSP00000282572.4:n.-130_-129del
NM_021147.4:c.-130_-129del NP_066970.3:n.-130_-129del
NR_125346.1:n.65_66del
NR_125347.1:n.65_66del