Canonical Allele Identifier: CA2728071413
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs2138326865
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48452961del , CM000675.2:g.48452961del GRCh38
NC_000013.10:g.49027097del , CM000675.1:g.49027097del GRCh37
NC_000013.9:g.47925098del NCBI36
NG_009009.1:g.154215del , LRG_517:g.154215del

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1696-32del MANE Select ENSP00000267163.4:n.1696-32del
ENST00000643064.1:c.194+71518del
ENST00000650461.1:c.1696-32del ENSP00000497193.1:n.1696-32del
ENST00000267163.4:c.1696-32del ENSP00000267163.4:n.1696-32del
ENST00000480491.1:n.395-32del
NM_000321.2:c.1696-32del , LRG_517t1:c.1696-32del NP_000312.2:n.1696-32del
XM_011535171.1:c.1435-32del XP_011533473.1:n.1435-32del
XM_011535171.2:c.1435-32del XP_011533473.1:n.1435-32del
NM_000321.3:c.1696-32del MANE Select NP_000312.2:n.1696-32del
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