Canonical Allele Identifier: CA2089950618

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48304135T= , CM000675.2:g.48304135T=	GRCh38
NC_000013.10:g.48878271T= , CM000675.1:g.48878271T=	GRCh37
NC_000013.9:g.47776272T=	NCBI36
NG_009009.1:g.5389T= , LRG_517:g.5389T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.137+86T= MANE Select	ENSP00000267163.4:n.137+86T=
ENST00000646097.1:c.137+86T=	ENSP00000496556.1:n.137+86T=
ENST00000650461.1:c.137+86T=	ENSP00000497193.1:n.137+86T=
ENST00000267163.4:c.137+86T=	ENSP00000267163.4:n.137+86T=
ENST00000467505.5:c.137+86T=	ENSP00000434702.1:n.137+86T=
ENST00000525036.1:n.299+86T=
NM_000321.2:c.137+86T= , LRG_517t1:c.137+86T=	NP_000312.2:n.137+86T=
NM_000321.3:c.137+86T= MANE Select	NP_000312.2:n.137+86T=