Canonical Allele Identifier: CA2089983840
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48368585C= , CM000675.2:g.48368585C= GRCh38
NC_000013.10:g.48942721C= , CM000675.1:g.48942721C= GRCh37
NC_000013.9:g.47840722C= NCBI36
NG_009009.1:g.69839C= , LRG_517:g.69839C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1108C= MANE Select ENSP00000267163.4:p.Pro370=
ENST00000650461.1:c.1108C= ENSP00000497193.1:p.Pro370=
ENST00000267163.4:c.1108C= ENSP00000267163.4:p.Pro370=
NM_000321.2:c.1108C= , LRG_517t1:c.1108C= NP_000312.2:p.Pro370=
XM_011535171.1:c.847C= XP_011533473.1:p.Pro283=
XM_011535171.2:c.847C= XP_011533473.1:p.Pro283=
XR_002957522.1:n.122-3609G=
NM_000321.3:c.1108C= MANE Select NP_000312.2:p.Pro370=