Canonical Allele Identifier: CA2687827953
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739711del , CM000670.2:g.86739711del GRCh38
NC_000008.10:g.87751939del , CM000670.1:g.87751939del GRCh37
NC_000008.9:g.87821055del NCBI36
NG_016980.1:g.8965del

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.155del MANE Select ENSP00000316605.5:p.Ser52PhefsTer?
ENST00000681746.1:c.155del ENSP00000505959.1:p.Ser52PhefsTer?
ENST00000320005.5:c.155del ENSP00000316605.5:p.Ser52PhefsTer?
ENST00000519777.1:n.137del
NM_019098.4:c.155del NP_061971.3:p.Ser52PhefsTer?
NM_019098.5:c.155del MANE Select NP_061971.3:p.Ser52PhefsTer?