Canonical Allele Identifier: CA2622977312
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48304010del , CM000675.2:g.48304010del GRCh38
NC_000013.10:g.48878146del , CM000675.1:g.48878146del GRCh37
NC_000013.9:g.47776147del NCBI36
NG_009009.1:g.5264del , LRG_517:g.5264del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.98del MANE Select ENSP00000267163.4:p.Pro33GlnfsTer?
ENST00000646097.1:c.98del ENSP00000496556.1:p.Pro33GlnfsTer?
ENST00000650461.1:c.98del ENSP00000497193.1:p.Pro33GlnfsTer?
ENST00000267163.4:c.98del ENSP00000267163.4:p.Pro33GlnfsTer?
ENST00000467505.5:c.98del ENSP00000434702.1:p.Pro33GlnfsTer?
ENST00000525036.1:n.260del
NM_000321.2:c.98del , LRG_517t1:c.98del NP_000312.2:p.Pro33GlnfsTer?
NM_000321.3:c.98del MANE Select NP_000312.2:p.Pro33GlnfsTer?