Canonical Allele Identifier: CA812219136

Gene: CCNO

Linked Data

• dbSNP Id: rs1271480617
• gnomAD v3: 5-55233619-G-C
• gnomAD v4: 5-55233619-G-C
• MyVariant Identifiers: chr5:g.54529447G>C (hg19) ; chr5:g.55233619G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233619G>C , CM000667.2:g.55233619G>C	GRCh38
NC_000005.9:g.54529447G>C , CM000667.1:g.54529447G>C	GRCh37
NC_000005.8:g.54565204G>C	NCBI36
NG_034201.1:g.5099C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.4:c.-96C>G	ENSP00000282572.4:n.-96C>G
NM_021147.4:c.-96C>G	NP_066970.3:n.-96C>G
NR_125346.1:n.99C>G
NR_125347.1:n.99C>G