Canonical Allele Identifier: CA2695218223
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303998dup , CM000675.2:g.48303998dup GRCh38
NC_000013.10:g.48878134dup , CM000675.1:g.48878134dup GRCh37
NC_000013.9:g.47776135dup NCBI36
NG_009009.1:g.5252dup , LRG_517:g.5252dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.86dup MANE Select ENSP00000267163.4:p.Glu30Ter
ENST00000646097.1:c.86dup ENSP00000496556.1:p.Glu30Ter
ENST00000650461.1:c.86dup ENSP00000497193.1:p.Glu30Ter
ENST00000267163.4:c.86dup ENSP00000267163.4:p.Glu30Ter
ENST00000467505.5:c.86dup ENSP00000434702.1:p.Glu30Ter
ENST00000525036.1:n.248dup
NM_000321.2:c.86dup , LRG_517t1:c.86dup NP_000312.2:p.Glu30Ter
NM_000321.3:c.86dup MANE Select NP_000312.2:p.Glu30Ter