Canonical Allele Identifier: CA359724204
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233196-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233196T>C , CM000667.2:g.55233196T>C GRCh38
NC_000005.9:g.54529024T>C , CM000667.1:g.54529024T>C GRCh37
NC_000005.8:g.54564781T>C NCBI36
NG_034201.1:g.5522A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.328A>G MANE Select ENSP00000282572.4:p.Lys110Glu
ENST00000282572.4:c.328A>G ENSP00000282572.4:p.Lys110Glu
ENST00000501463.2:c.328A>G ENSP00000422485.1:p.Lys110Glu
NM_021147.4:c.328A>G NP_066970.3:p.Lys110Glu
NR_125346.1:n.522A>G
NR_125347.1:n.522A>G
NM_021147.5:c.328A>G MANE Select NP_066970.3:p.Lys110Glu
NR_125346.2:n.413A>G
NR_125347.2:n.413A>G