Canonical Allele Identifier: CA2622985069
Gene: RB1 HGNC NCBI

Linked Data

gnomAD v4: 13-48459601-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459601T>A , CM000675.2:g.48459601T>A GRCh38
NC_000013.10:g.49033737T>A , CM000675.1:g.49033737T>A GRCh37
NC_000013.9:g.47931738T>A NCBI36
NG_009009.1:g.160855T>A , LRG_517:g.160855T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1961-87T>A MANE Select ENSP00000267163.4:n.1961-87T>A
ENST00000643064.1:c.194+78158T>A
ENST00000650461.1:c.1961-87T>A ENSP00000497193.1:n.1961-87T>A
ENST00000267163.4:c.1961-87T>A ENSP00000267163.4:n.1961-87T>A
NM_000321.2:c.1961-87T>A , LRG_517t1:c.1961-87T>A NP_000312.2:n.1961-87T>A
XM_011535171.1:c.1700-87T>A XP_011533473.1:n.1700-87T>A
XM_011535171.2:c.1700-87T>A XP_011533473.1:n.1700-87T>A
NM_000321.3:c.1961-87T>A MANE Select NP_000312.2:n.1961-87T>A
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