Canonical Allele Identifier: CA2673856972
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1745675085
gnomAD v4: 5-55233654-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233654T>C , CM000667.2:g.55233654T>C GRCh38
NC_000005.9:g.54529482T>C , CM000667.1:g.54529482T>C GRCh37
NC_000005.8:g.54565239T>C NCBI36
NG_034201.1:g.5064A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-131A>G ENSP00000282572.4:n.-131A>G
NM_021147.4:c.-131A>G NP_066970.3:n.-131A>G
NR_125346.1:n.64A>G
NR_125347.1:n.64A>G