Canonical Allele Identifier: CA2089982387
Gene: RB1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.937G= MANE Select ENSP00000267163.4:p.Glu313=
ENST00000650461.1:c.937G= ENSP00000497193.1:p.Glu313=
ENST00000267163.4:c.937G= ENSP00000267163.4:p.Glu313=
NM_000321.2:c.937G= , LRG_517t1:c.937G= NP_000312.2:p.Glu313=
XM_011535171.1:c.676G= XP_011533473.1:p.Glu226=
XM_011535171.2:c.676G= XP_011533473.1:p.Glu226=
XR_002957522.1:n.129C=
NM_000321.3:c.937G= MANE Select NP_000312.2:p.Glu313=