Canonical Allele Identifier: CA2089949679
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs1952050380
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303862C>G , CM000675.2:g.48303862C>G GRCh38
NC_000013.10:g.48877998C>G , CM000675.1:g.48877998C>G GRCh37
NC_000013.9:g.47775999C>G NCBI36
NG_009009.1:g.5116C>G , LRG_517:g.5116C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.-51C>G MANE Select ENSP00000267163.4:n.-51C>G
ENST00000646097.1:c.-51C>G ENSP00000496556.1:n.-51C>G
ENST00000650461.1:c.-51C>G ENSP00000497193.1:n.-51C>G
ENST00000267163.4:c.-51C>G ENSP00000267163.4:n.-51C>G
ENST00000467505.5:c.-51C>G ENSP00000434702.1:n.-51C>G
ENST00000525036.1:n.112C>G
NM_000321.2:c.-51C>G , LRG_517t1:c.-51C>G NP_000312.2:n.-51C>G
NM_000321.3:c.-51C>G MANE Select NP_000312.2:n.-51C>G
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