Canonical Allele Identifier: CA1547396580

Gene: CCNO

Linked Data

• dbSNP Id: rs1225361838

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232994G>C , CM000667.2:g.55232994G>C	GRCh38
NC_000005.9:g.54528822G>C , CM000667.1:g.54528822G>C	GRCh37
NC_000005.8:g.54564579G>C	NCBI36
NG_034201.1:g.5724C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+149C>G MANE Select	ENSP00000282572.4:n.381+149C>G
ENST00000282572.4:c.381+149C>G	ENSP00000282572.4:n.381+149C>G
ENST00000501463.2:c.*134C>G	ENSP00000422485.1:n.*134C>G
NM_021147.4:c.381+149C>G	NP_066970.3:n.381+149C>G
NR_125346.1:n.724C>G
NR_125347.1:n.580+144C>G
NM_021147.5:c.381+149C>G MANE Select	NP_066970.3:n.381+149C>G
NR_125346.2:n.615C>G
NR_125347.2:n.471+144C>G