Canonical Allele Identifier: CA2728030258
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs2138026396

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303813del , CM000675.2:g.48303813del GRCh38
NC_000013.10:g.48877949del , CM000675.1:g.48877949del GRCh37
NC_000013.9:g.47775950del NCBI36
NG_009009.1:g.5067del , LRG_517:g.5067del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.-100del MANE Select ENSP00000267163.4:n.-100del
ENST00000646097.1:c.-100del ENSP00000496556.1:n.-100del
ENST00000650461.1:c.-100del ENSP00000497193.1:n.-100del
ENST00000267163.4:c.-100del ENSP00000267163.4:n.-100del
ENST00000467505.5:c.-100del ENSP00000434702.1:n.-100del
ENST00000525036.1:n.63del
NM_000321.2:c.-100del , LRG_517t1:c.-100del NP_000312.2:n.-100del
NM_000321.3:c.-100del MANE Select NP_000312.2:n.-100del