Canonical Allele Identifier: CA2090013965
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs1593529830

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48452938A>G , CM000675.2:g.48452938A>G GRCh38
NC_000013.10:g.49027074A>G , CM000675.1:g.49027074A>G GRCh37
NC_000013.9:g.47925075A>G NCBI36
NG_009009.1:g.154192A>G , LRG_517:g.154192A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1696-55A>G MANE Select ENSP00000267163.4:n.1696-55A>G
ENST00000643064.1:c.194+71495A>G
ENST00000650461.1:c.1696-55A>G ENSP00000497193.1:n.1696-55A>G
ENST00000267163.4:c.1696-55A>G ENSP00000267163.4:n.1696-55A>G
ENST00000480491.1:n.395-55A>G
NM_000321.2:c.1696-55A>G , LRG_517t1:c.1696-55A>G NP_000312.2:n.1696-55A>G
XM_011535171.1:c.1435-55A>G XP_011533473.1:n.1435-55A>G
XM_011535171.2:c.1435-55A>G XP_011533473.1:n.1435-55A>G
NM_000321.3:c.1696-55A>G MANE Select NP_000312.2:n.1696-55A>G