Canonical Allele Identifier: CA388163522
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs2138145123

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48381309C>A , CM000675.2:g.48381309C>A GRCh38
NC_000013.10:g.48955445C>A , CM000675.1:g.48955445C>A GRCh37
NC_000013.9:g.47853446C>A NCBI36
NG_009009.1:g.82563C>A , LRG_517:g.82563C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1561C>A MANE Select ENSP00000267163.4:p.Leu521Ile
ENST00000643064.1:c.60C>A
ENST00000650461.1:c.1561C>A ENSP00000497193.1:p.Leu521Ile
ENST00000267163.4:c.1561C>A ENSP00000267163.4:p.Leu521Ile
NM_000321.2:c.1561C>A , LRG_517t1:c.1561C>A NP_000312.2:p.Leu521Ile
XM_011535171.1:c.1300C>A XP_011533473.1:p.Leu434Ile
XM_011535171.2:c.1300C>A XP_011533473.1:p.Leu434Ile
NM_000321.3:c.1561C>A MANE Select NP_000312.2:p.Leu521Ile