Canonical Allele Identifier: CA2089972201
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48381230T= , CM000675.2:g.48381230T= GRCh38
NC_000013.10:g.48955366T= , CM000675.1:g.48955366T= GRCh37
NC_000013.9:g.47853367T= NCBI36
NG_009009.1:g.82484T= , LRG_517:g.82484T=

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1499-17T= MANE Select ENSP00000267163.4:n.1499-17T=
ENST00000650461.1:c.1499-17T= ENSP00000497193.1:n.1499-17T=
ENST00000267163.4:c.1499-17T= ENSP00000267163.4:n.1499-17T=
NM_000321.2:c.1499-17T= , LRG_517t1:c.1499-17T= NP_000312.2:n.1499-17T=
XM_011535171.1:c.1238-17T= XP_011533473.1:n.1238-17T=
XM_011535171.2:c.1238-17T= XP_011533473.1:n.1238-17T=
NM_000321.3:c.1499-17T= MANE Select NP_000312.2:n.1499-17T=