Canonical Allele Identifier: CA2673856478
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233077-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233077G>T , CM000667.2:g.55233077G>T GRCh38
NC_000005.9:g.54528905G>T , CM000667.1:g.54528905G>T GRCh37
NC_000005.8:g.54564662G>T NCBI36
NG_034201.1:g.5641C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+66C>A MANE Select ENSP00000282572.4:n.381+66C>A
ENST00000282572.4:c.381+66C>A ENSP00000282572.4:n.381+66C>A
ENST00000501463.2:c.*51C>A ENSP00000422485.1:n.*51C>A
NM_021147.4:c.381+66C>A NP_066970.3:n.381+66C>A
NR_125346.1:n.641C>A
NR_125347.1:n.580+61C>A
NM_021147.5:c.381+66C>A MANE Select NP_066970.3:n.381+66C>A
NR_125346.2:n.532C>A
NR_125347.2:n.471+61C>A
Search 100 bp 5'
Search 100 bp 3'