Canonical Allele Identifier: CA2695218615
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459693_48459694insAT , CM000675.2:g.48459693_48459694insAT GRCh38
NC_000013.10:g.49033829_49033830insAT , CM000675.1:g.49033829_49033830insAT GRCh37
NC_000013.9:g.47931830_47931831insAT NCBI36
NG_009009.1:g.160947_160948insAT , LRG_517:g.160947_160948insAT

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1966_1967insAT MANE Select ENSP00000267163.4:p.Arg656HisfsTer3
ENST00000643064.1:c.194+78250_194+78251insAT
ENST00000650461.1:c.1966_1967insAT ENSP00000497193.1:p.Arg656HisfsTer3
ENST00000267163.4:c.1966_1967insAT ENSP00000267163.4:p.Arg656HisfsTer3
NM_000321.2:c.1966_1967insAT , LRG_517t1:c.1966_1967insAT NP_000312.2:p.Arg656HisfsTer3
XM_011535171.1:c.1705_1706insAT XP_011533473.1:p.Arg569HisfsTer3
XM_011535171.2:c.1705_1706insAT XP_011533473.1:p.Arg569HisfsTer3
NM_000321.3:c.1966_1967insAT MANE Select NP_000312.2:p.Arg656HisfsTer3