Canonical Allele Identifier: CA2089982338
Gene: RB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48364865T= , CM000675.2:g.48364865T= GRCh38
NC_000013.10:g.48939001T= , CM000675.1:g.48939001T= GRCh37
NC_000013.9:g.47837002T= NCBI36
NG_009009.1:g.66119T= , LRG_517:g.66119T=

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.862-29T= MANE Select ENSP00000267163.4:n.862-29T=
ENST00000650461.1:c.862-29T= ENSP00000497193.1:n.862-29T=
ENST00000267163.4:c.862-29T= ENSP00000267163.4:n.862-29T=
NM_000321.2:c.862-29T= , LRG_517t1:c.862-29T= NP_000312.2:n.862-29T=
XM_011535171.1:c.601-29T= XP_011533473.1:n.601-29T=
XM_011535171.2:c.601-29T= XP_011533473.1:n.601-29T=
NM_000321.3:c.862-29T= MANE Select NP_000312.2:n.862-29T=
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