Canonical Allele Identifier: CA2673856303
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232928-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232928G>A , CM000667.2:g.55232928G>A GRCh38
NC_000005.9:g.54528756G>A , CM000667.1:g.54528756G>A GRCh37
NC_000005.8:g.54564513G>A NCBI36
NG_034201.1:g.5790C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+215C>T MANE Select ENSP00000282572.4:n.381+215C>T
ENST00000282572.4:c.381+215C>T ENSP00000282572.4:n.381+215C>T
ENST00000501463.2:c.*200C>T ENSP00000422485.1:n.*200C>T
NM_021147.4:c.381+215C>T NP_066970.3:n.381+215C>T
NR_125346.1:n.790C>T
NR_125347.1:n.580+210C>T
NR_125348.1:n.64C>T
NM_021147.5:c.381+215C>T MANE Select NP_066970.3:n.381+215C>T
NR_125346.2:n.681C>T
NR_125347.2:n.471+210C>T