Canonical Allele Identifier: CA2728089931
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs2138335648

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459642del , CM000675.2:g.48459642del GRCh38
NC_000013.10:g.49033778del , CM000675.1:g.49033778del GRCh37
NC_000013.9:g.47931779del NCBI36
NG_009009.1:g.160896del , LRG_517:g.160896del

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1961-46del MANE Select ENSP00000267163.4:n.1961-46del
ENST00000643064.1:c.194+78199del
ENST00000650461.1:c.1961-46del ENSP00000497193.1:n.1961-46del
ENST00000267163.4:c.1961-46del ENSP00000267163.4:n.1961-46del
NM_000321.2:c.1961-46del , LRG_517t1:c.1961-46del NP_000312.2:n.1961-46del
XM_011535171.1:c.1700-46del XP_011533473.1:n.1700-46del
XM_011535171.2:c.1700-46del XP_011533473.1:n.1700-46del
NM_000321.3:c.1961-46del MANE Select NP_000312.2:n.1961-46del