Canonical Allele Identifier: CA2673856457
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233060-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233060G>T , CM000667.2:g.55233060G>T GRCh38
NC_000005.9:g.54528888G>T , CM000667.1:g.54528888G>T GRCh37
NC_000005.8:g.54564645G>T NCBI36
NG_034201.1:g.5658C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+83C>A MANE Select ENSP00000282572.4:n.381+83C>A
ENST00000282572.4:c.381+83C>A ENSP00000282572.4:n.381+83C>A
ENST00000501463.2:c.*68C>A ENSP00000422485.1:n.*68C>A
NM_021147.4:c.381+83C>A NP_066970.3:n.381+83C>A
NR_125346.1:n.658C>A
NR_125347.1:n.580+78C>A
NM_021147.5:c.381+83C>A MANE Select NP_066970.3:n.381+83C>A
NR_125346.2:n.549C>A
NR_125347.2:n.471+78C>A
Search 100 bp 5'
Search 100 bp 3'