Canonical Allele Identifier: CA2090019525
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459688T= , CM000675.2:g.48459688T= GRCh38
NC_000013.10:g.49033824T= , CM000675.1:g.49033824T= GRCh37
NC_000013.9:g.47931825T= NCBI36
NG_009009.1:g.160942T= , LRG_517:g.160942T=

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1961T= MANE Select ENSP00000267163.4:p.Val654=
ENST00000643064.1:c.194+78245T=
ENST00000650461.1:c.1961T= ENSP00000497193.1:p.Val654=
ENST00000267163.4:c.1961T= ENSP00000267163.4:p.Val654=
NM_000321.2:c.1961T= , LRG_517t1:c.1961T= NP_000312.2:p.Val654=
XM_011535171.1:c.1700T= XP_011533473.1:p.Val567=
XM_011535171.2:c.1700T= XP_011533473.1:p.Val567=
NM_000321.3:c.1961T= MANE Select NP_000312.2:p.Val654=