Canonical Allele Identifier: CA2090013910

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48452858T= , CM000675.2:g.48452858T=	GRCh38
NC_000013.10:g.49026994T= , CM000675.1:g.49026994T=	GRCh37
NC_000013.9:g.47924995T=	NCBI36
NG_009009.1:g.154112T= , LRG_517:g.154112T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.1696-135T= MANE Select	ENSP00000267163.4:n.1696-135T=
ENST00000643064.1:c.194+71415T=
ENST00000650461.1:c.1696-135T=	ENSP00000497193.1:n.1696-135T=
ENST00000267163.4:c.1696-135T=	ENSP00000267163.4:n.1696-135T=
ENST00000480491.1:n.395-135T=
NM_000321.2:c.1696-135T= , LRG_517t1:c.1696-135T=	NP_000312.2:n.1696-135T=
XM_011535171.1:c.1435-135T=	XP_011533473.1:n.1435-135T=
XM_011535171.2:c.1435-135T=	XP_011533473.1:n.1435-135T=
NM_000321.3:c.1696-135T= MANE Select	NP_000312.2:n.1696-135T=