Canonical Allele Identifier: CA388160092
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs587778843

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48364969G>A , CM000675.2:g.48364969G>A GRCh38
NC_000013.10:g.48939105G>A , CM000675.1:g.48939105G>A GRCh37
NC_000013.9:g.47837106G>A NCBI36
NG_009009.1:g.66223G>A , LRG_517:g.66223G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.937G>A MANE Select ENSP00000267163.4:p.Glu313Lys
ENST00000650461.1:c.937G>A ENSP00000497193.1:p.Glu313Lys
ENST00000267163.4:c.937G>A ENSP00000267163.4:p.Glu313Lys
NM_000321.2:c.937G>A , LRG_517t1:c.937G>A NP_000312.2:p.Glu313Lys
XM_011535171.1:c.676G>A XP_011533473.1:p.Glu226Lys
XM_011535171.2:c.676G>A XP_011533473.1:p.Glu226Lys
XR_002957522.1:n.129C>T
NM_000321.3:c.937G>A MANE Select NP_000312.2:p.Glu313Lys