Canonical Allele Identifier: CA2089971082
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48380111T= , CM000675.2:g.48380111T= GRCh38
NC_000013.10:g.48954247T= , CM000675.1:g.48954247T= GRCh37
NC_000013.9:g.47852248T= NCBI36
NG_009009.1:g.81365T= , LRG_517:g.81365T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1421+27T= MANE Select ENSP00000267163.4:n.1421+27T=
ENST00000650461.1:c.1421+27T= ENSP00000497193.1:n.1421+27T=
ENST00000267163.4:c.1421+27T= ENSP00000267163.4:n.1421+27T=
NM_000321.2:c.1421+27T= , LRG_517t1:c.1421+27T= NP_000312.2:n.1421+27T=
XM_011535171.1:c.1160+27T= XP_011533473.1:n.1160+27T=
XM_011535171.2:c.1160+27T= XP_011533473.1:n.1160+27T=
NM_000321.3:c.1421+27T= MANE Select NP_000312.2:n.1421+27T=