Canonical Allele Identifier: CA2089950222

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303991C= , CM000675.2:g.48303991C=	GRCh38
NC_000013.10:g.48878127C= , CM000675.1:g.48878127C=	GRCh37
NC_000013.9:g.47776128C=	NCBI36
NG_009009.1:g.5245C= , LRG_517:g.5245C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.79C= MANE Select	ENSP00000267163.4:p.Pro27=
ENST00000646097.1:c.79C=	ENSP00000496556.1:p.Pro27=
ENST00000650461.1:c.79C=	ENSP00000497193.1:p.Pro27=
ENST00000267163.4:c.79C=	ENSP00000267163.4:p.Pro27=
ENST00000467505.5:c.79C=	ENSP00000434702.1:p.Pro27=
ENST00000525036.1:n.241C=
NM_000321.2:c.79C= , LRG_517t1:c.79C=	NP_000312.2:p.Pro27=
NM_000321.3:c.79C= MANE Select	NP_000312.2:p.Pro27=