Canonical Allele Identifier: CA2622980161
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48364975del , CM000675.2:g.48364975del GRCh38
NC_000013.10:g.48939111del , CM000675.1:g.48939111del GRCh37
NC_000013.9:g.47837112del NCBI36
NG_009009.1:g.66229del , LRG_517:g.66229del

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.939+4del MANE Select ENSP00000267163.4:n.939+4del
ENST00000650461.1:c.939+4del ENSP00000497193.1:n.939+4del
ENST00000267163.4:c.939+4del ENSP00000267163.4:n.939+4del
NM_000321.2:c.939+4del , LRG_517t1:c.939+4del NP_000312.2:n.939+4del
XM_011535171.1:c.678+4del XP_011533473.1:n.678+4del
XM_011535171.2:c.678+4del XP_011533473.1:n.678+4del
XR_002957522.1:n.124del
NM_000321.3:c.939+4del MANE Select NP_000312.2:n.939+4del