Canonical Allele Identifier: CA2622977241
Gene: RB1 HGNC NCBI

Linked Data

gnomAD v4: 13-48303862-C-A
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Genomic Alleles

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

Transcript Alleles

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