Canonical Allele Identifier: CA2695218485
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48380237del , CM000675.2:g.48380237del GRCh38
NC_000013.10:g.48954373del , CM000675.1:g.48954373del GRCh37
NC_000013.9:g.47852374del NCBI36
NG_009009.1:g.81491del , LRG_517:g.81491del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1494del MANE Select ENSP00000267163.4:p.Tyr498Ter
ENST00000650461.1:c.1494del ENSP00000497193.1:p.Tyr498Ter
ENST00000267163.4:c.1494del ENSP00000267163.4:p.Tyr498Ter
NM_000321.2:c.1494del , LRG_517t1:c.1494del NP_000312.2:p.Tyr498Ter
XM_011535171.1:c.1233del XP_011533473.1:p.Tyr411Ter
XM_011535171.2:c.1233del XP_011533473.1:p.Tyr411Ter
NM_000321.3:c.1494del MANE Select NP_000312.2:p.Tyr498Ter