Canonical Allele Identifier: CA2089983835

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48368570G= , CM000675.2:g.48368570G=	GRCh38
NC_000013.10:g.48942706G= , CM000675.1:g.48942706G=	GRCh37
NC_000013.9:g.47840707G=	NCBI36
NG_009009.1:g.69824G= , LRG_517:g.69824G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1093G= MANE Select	ENSP00000267163.4:p.Glu365=
ENST00000650461.1:c.1093G=	ENSP00000497193.1:p.Glu365=
ENST00000267163.4:c.1093G=	ENSP00000267163.4:p.Glu365=
NM_000321.2:c.1093G= , LRG_517t1:c.1093G=	NP_000312.2:p.Glu365=
XM_011535171.1:c.832G=	XP_011533473.1:p.Glu278=
XM_011535171.2:c.832G=	XP_011533473.1:p.Glu278=
XR_002957522.1:n.122-3594C=
NM_000321.3:c.1093G= MANE Select	NP_000312.2:p.Glu365=