Canonical Allele Identifier: CA2089949549
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303761C= , CM000675.2:g.48303761C= GRCh38
NC_000013.10:g.48877897C= , CM000675.1:g.48877897C= GRCh37
NC_000013.9:g.47775898C= NCBI36
NG_009009.1:g.5015C= , LRG_517:g.5015C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.-152C= MANE Select ENSP00000267163.4:n.-152C=
ENST00000646097.1:c.-152C= ENSP00000496556.1:n.-152C=
ENST00000650461.1:c.-152C= ENSP00000497193.1:n.-152C=
ENST00000525036.1:n.11C=
NM_000321.2:c.-152C= , LRG_517t1:c.-152C= NP_000312.2:n.-152C=
NM_000321.3:c.-152C= MANE Select NP_000312.2:n.-152C=