Canonical Allele Identifier: CA2728038621
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs2138028617

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48304142_48304144del , CM000675.2:g.48304142_48304144del GRCh38
NC_000013.10:g.48878278_48878280del , CM000675.1:g.48878278_48878280del GRCh37
NC_000013.9:g.47776279_47776281del NCBI36
NG_009009.1:g.5396_5398del , LRG_517:g.5396_5398del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.137+93_137+95del MANE Select ENSP00000267163.4:n.137+93_137+95del
ENST00000646097.1:c.137+93_137+95del ENSP00000496556.1:n.137+93_137+95del
ENST00000650461.1:c.137+93_137+95del ENSP00000497193.1:n.137+93_137+95del
ENST00000267163.4:c.137+93_137+95del ENSP00000267163.4:n.137+93_137+95del
ENST00000467505.5:c.137+93_137+95del ENSP00000434702.1:n.137+93_137+95del
ENST00000525036.1:n.299+93_299+95del
NM_000321.2:c.137+93_137+95del , LRG_517t1:c.137+93_137+95del NP_000312.2:n.137+93_137+95del
NM_000321.3:c.137+93_137+95del MANE Select NP_000312.2:n.137+93_137+95del