Canonical Allele Identifier: CA2622977301
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303957_48303985del , CM000675.2:g.48303957_48303985del GRCh38
NC_000013.10:g.48878093_48878121del , CM000675.1:g.48878093_48878121del GRCh37
NC_000013.9:g.47776094_47776122del NCBI36
NG_009009.1:g.5211_5239del , LRG_517:g.5211_5239del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.45_73del MANE Select ENSP00000267163.4:p.Ala18ProfsTer3
ENST00000646097.1:c.45_73del ENSP00000496556.1:p.Ala18ProfsTer3
ENST00000650461.1:c.45_73del ENSP00000497193.1:p.Ala18ProfsTer3
ENST00000267163.4:c.45_73del ENSP00000267163.4:p.Ala18ProfsTer3
ENST00000467505.5:c.45_73del ENSP00000434702.1:p.Ala18ProfsTer3
ENST00000525036.1:n.207_235del
NM_000321.2:c.45_73del , LRG_517t1:c.45_73del NP_000312.2:p.Ala18ProfsTer3
NM_000321.3:c.45_73del MANE Select NP_000312.2:p.Ala18ProfsTer3