Canonical Allele Identifier: CA2622977224
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs2138026625
gnomAD v4: 13-48303852-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303852C>A , CM000675.2:g.48303852C>A GRCh38
NC_000013.10:g.48877988C>A , CM000675.1:g.48877988C>A GRCh37
NC_000013.9:g.47775989C>A NCBI36
NG_009009.1:g.5106C>A , LRG_517:g.5106C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.-61C>A MANE Select ENSP00000267163.4:n.-61C>A
ENST00000646097.1:c.-61C>A ENSP00000496556.1:n.-61C>A
ENST00000650461.1:c.-61C>A ENSP00000497193.1:n.-61C>A
ENST00000267163.4:c.-61C>A ENSP00000267163.4:n.-61C>A
ENST00000467505.5:c.-61C>A ENSP00000434702.1:n.-61C>A
ENST00000525036.1:n.102C>A
NM_000321.2:c.-61C>A , LRG_517t1:c.-61C>A NP_000312.2:n.-61C>A
NM_000321.3:c.-61C>A MANE Select NP_000312.2:n.-61C>A
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