Canonical Allele Identifier: CA2695209887
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579210del , CM000670.2:g.86579210del GRCh38
NC_000008.10:g.87591438del , CM000670.1:g.87591438del GRCh37
NC_000008.9:g.87660554del NCBI36
NG_016980.1:g.169467del

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1825del MANE Select ENSP00000316605.5:p.Val609TrpfsTer9
ENST00000681546.1:n.1645del
ENST00000681746.1:c.*236del ENSP00000505959.1:n.*236del
ENST00000320005.5:c.1825del ENSP00000316605.5:p.Val609TrpfsTer9
NM_019098.4:c.1825del NP_061971.3:p.Val609TrpfsTer9
XM_011517138.1:c.1411del XP_011515440.1:p.Val471TrpfsTer9
XM_011517138.2:c.1411del XP_011515440.1:p.Val471TrpfsTer9
NM_019098.5:c.1825del MANE Select NP_061971.3:p.Val609TrpfsTer9