Canonical Allele Identifier: CA2089949511
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303751A= , CM000675.2:g.48303751A= GRCh38
NC_000013.10:g.48877887A= , CM000675.1:g.48877887A= GRCh37
NC_000013.9:g.47775888A= NCBI36
NG_009009.1:g.5005A= , LRG_517:g.5005A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.-162A= MANE Select ENSP00000267163.4:n.-162A=
ENST00000646097.1:c.-162A= ENSP00000496556.1:n.-162A=
ENST00000650461.1:c.-162A= ENSP00000497193.1:n.-162A=
ENST00000525036.1:n.1A=
NM_000321.2:c.-162A= , LRG_517t1:c.-162A= NP_000312.2:n.-162A=
NM_000321.3:c.-162A= MANE Select NP_000312.2:n.-162A=