Canonical Allele Identifier: CA2673856305
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232930-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232930C>A , CM000667.2:g.55232930C>A GRCh38
NC_000005.9:g.54528758C>A , CM000667.1:g.54528758C>A GRCh37
NC_000005.8:g.54564515C>A NCBI36
NG_034201.1:g.5788G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+213G>T MANE Select ENSP00000282572.4:n.381+213G>T
ENST00000282572.4:c.381+213G>T ENSP00000282572.4:n.381+213G>T
ENST00000501463.2:c.*198G>T ENSP00000422485.1:n.*198G>T
NM_021147.4:c.381+213G>T NP_066970.3:n.381+213G>T
NR_125346.1:n.788G>T
NR_125347.1:n.580+208G>T
NR_125348.1:n.62G>T
NM_021147.5:c.381+213G>T MANE Select NP_066970.3:n.381+213G>T
NR_125346.2:n.679G>T
NR_125347.2:n.471+208G>T