Canonical Allele Identifier: CA2090019406
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs1949382499

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459566del , CM000675.2:g.48459566del GRCh38
NC_000013.10:g.49033702del , CM000675.1:g.49033702del GRCh37
NC_000013.9:g.47931703del NCBI36
NG_009009.1:g.160820del , LRG_517:g.160820del

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1961-122del MANE Select ENSP00000267163.4:n.1961-122del
ENST00000643064.1:c.194+78123del
ENST00000650461.1:c.1961-122del ENSP00000497193.1:n.1961-122del
ENST00000267163.4:c.1961-122del ENSP00000267163.4:n.1961-122del
NM_000321.2:c.1961-122del , LRG_517t1:c.1961-122del NP_000312.2:n.1961-122del
XM_011535171.1:c.1700-122del XP_011533473.1:n.1700-122del
XM_011535171.2:c.1700-122del XP_011533473.1:n.1700-122del
NM_000321.3:c.1961-122del MANE Select NP_000312.2:n.1961-122del