Canonical Allele Identifier: CA2578309983
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233618-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233618G>C , CM000667.2:g.55233618G>C GRCh38
NC_000005.9:g.54529446G>C , CM000667.1:g.54529446G>C GRCh37
NC_000005.8:g.54565203G>C NCBI36
NG_034201.1:g.5100C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-95C>G ENSP00000282572.4:n.-95C>G
NM_021147.4:c.-95C>G NP_066970.3:n.-95C>G
NR_125346.1:n.100C>G
NR_125347.1:n.100C>G