Canonical Allele Identifier: CA1547391120

Gene: CCNO

Linked Data

• dbSNP Id: rs1745676744

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233692G>C , CM000667.2:g.55233692G>C	GRCh38
NC_000005.9:g.54529520G>C , CM000667.1:g.54529520G>C	GRCh37
NC_000005.8:g.54565277G>C	NCBI36
NG_034201.1:g.5026C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_021147.4:c.-169C>G	NP_066970.3:n.-169C>G
NR_125346.1:n.26C>G
NR_125347.1:n.26C>G