Canonical Allele Identifier: CA2673856292
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232917-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232917A>G , CM000667.2:g.55232917A>G GRCh38
NC_000005.9:g.54528745A>G , CM000667.1:g.54528745A>G GRCh37
NC_000005.8:g.54564502A>G NCBI36
NG_034201.1:g.5801T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+226T>C MANE Select ENSP00000282572.4:n.381+226T>C
ENST00000282572.4:c.381+226T>C ENSP00000282572.4:n.381+226T>C
ENST00000501463.2:c.*211T>C ENSP00000422485.1:n.*211T>C
NM_021147.4:c.381+226T>C NP_066970.3:n.381+226T>C
NR_125346.1:n.801T>C
NR_125347.1:n.580+221T>C
NR_125348.1:n.75T>C
NM_021147.5:c.381+226T>C MANE Select NP_066970.3:n.381+226T>C
NR_125346.2:n.692T>C
NR_125347.2:n.471+221T>C
Search 100 bp 5'
Search 100 bp 3'