Canonical Allele Identifier: CA2090008018

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48459743G= , CM000675.2:g.48459743G=	GRCh38
NC_000013.10:g.49033879G= , CM000675.1:g.49033879G=	GRCh37
NC_000013.9:g.47931880G=	NCBI36
NG_009009.1:g.160997G= , LRG_517:g.160997G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2016G= MANE Select	ENSP00000267163.4:p.Glu672=
ENST00000643064.1:c.194+78300G=
ENST00000650461.1:c.2016G=	ENSP00000497193.1:p.Glu672=
ENST00000267163.4:c.2016G=	ENSP00000267163.4:p.Glu672=
NM_000321.2:c.2016G= , LRG_517t1:c.2016G=	NP_000312.2:p.Glu672=
XM_011535171.1:c.1755G=	XP_011533473.1:p.Glu585=
XM_011535171.2:c.1755G=	XP_011533473.1:p.Glu585=
NM_000321.3:c.2016G= MANE Select	NP_000312.2:p.Glu672=