Canonical Allele Identifier: CA388252654
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs121913296

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48345108G>A , CM000675.2:g.48345108G>A GRCh38
NC_000013.10:g.48919244G>A , CM000675.1:g.48919244G>A GRCh37
NC_000013.9:g.47817245G>A NCBI36
NG_009009.1:g.46362G>A , LRG_517:g.46362G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.409G>A MANE Select ENSP00000267163.4:p.Glu137Lys
ENST00000650461.1:c.409G>A ENSP00000497193.1:p.Glu137Lys
ENST00000267163.4:c.409G>A ENSP00000267163.4:p.Glu137Lys
ENST00000467505.5:c.138-14909G>A ENSP00000434702.1:n.138-14909G>A
ENST00000525036.1:n.571G>A
NM_000321.2:c.409G>A , LRG_517t1:c.409G>A NP_000312.2:p.Glu137Lys
XM_011535171.1:c.148G>A XP_011533473.1:p.Glu50Lys
XM_011535171.2:c.148G>A XP_011533473.1:p.Glu50Lys
NM_000321.3:c.409G>A MANE Select NP_000312.2:p.Glu137Lys