Canonical Allele Identifier: CA2673856490
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233085-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233085G>T , CM000667.2:g.55233085G>T GRCh38
NC_000005.9:g.54528913G>T , CM000667.1:g.54528913G>T GRCh37
NC_000005.8:g.54564670G>T NCBI36
NG_034201.1:g.5633C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+58C>A MANE Select ENSP00000282572.4:n.381+58C>A
ENST00000282572.4:c.381+58C>A ENSP00000282572.4:n.381+58C>A
ENST00000501463.2:c.*43C>A ENSP00000422485.1:n.*43C>A
NM_021147.4:c.381+58C>A NP_066970.3:n.381+58C>A
NR_125346.1:n.633C>A
NR_125347.1:n.580+53C>A
NM_021147.5:c.381+58C>A MANE Select NP_066970.3:n.381+58C>A
NR_125346.2:n.524C>A
NR_125347.2:n.471+53C>A
Search 100 bp 5'
Search 100 bp 3'