Canonical Allele Identifier: CA2673856855
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233567-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233567G>C , CM000667.2:g.55233567G>C GRCh38
NC_000005.9:g.54529395G>C , CM000667.1:g.54529395G>C GRCh37
NC_000005.8:g.54565152G>C NCBI36
NG_034201.1:g.5151C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-44C>G MANE Select ENSP00000282572.4:n.-44C>G
ENST00000282572.4:c.-44C>G ENSP00000282572.4:n.-44C>G
ENST00000501463.2:c.-44C>G ENSP00000422485.1:n.-44C>G
NM_021147.4:c.-44C>G NP_066970.3:n.-44C>G
NR_125346.1:n.151C>G
NR_125347.1:n.151C>G
NM_021147.5:c.-44C>G MANE Select NP_066970.3:n.-44C>G
NR_125346.2:n.42C>G
NR_125347.2:n.42C>G