Canonical Allele Identifier: CA2089982435
Gene: RB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48365073T= , CM000675.2:g.48365073T= GRCh38
NC_000013.10:g.48939209T= , CM000675.1:g.48939209T= GRCh37
NC_000013.9:g.47837210T= NCBI36
NG_009009.1:g.66327T= , LRG_517:g.66327T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.939+102T= MANE Select ENSP00000267163.4:n.939+102T=
ENST00000650461.1:c.939+102T= ENSP00000497193.1:n.939+102T=
ENST00000267163.4:c.939+102T= ENSP00000267163.4:n.939+102T=
NM_000321.2:c.939+102T= , LRG_517t1:c.939+102T= NP_000312.2:n.939+102T=
XM_011535171.1:c.678+102T= XP_011533473.1:n.678+102T=
XM_011535171.2:c.678+102T= XP_011533473.1:n.678+102T=
XR_002957522.1:n.122-97A=
NM_000321.3:c.939+102T= MANE Select NP_000312.2:n.939+102T=
Search 100 bp 5'
Search 100 bp 3'