Canonical Allele Identifier: CA2089982385

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48364961G= , CM000675.2:g.48364961G=	GRCh38
NC_000013.10:g.48939097G= , CM000675.1:g.48939097G=	GRCh37
NC_000013.9:g.47837098G=	NCBI36
NG_009009.1:g.66215G= , LRG_517:g.66215G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.929G= MANE Select	ENSP00000267163.4:p.Gly310=
ENST00000650461.1:c.929G=	ENSP00000497193.1:p.Gly310=
ENST00000267163.4:c.929G=	ENSP00000267163.4:p.Gly310=
NM_000321.2:c.929G= , LRG_517t1:c.929G=	NP_000312.2:p.Gly310=
XM_011535171.1:c.668G=	XP_011533473.1:p.Gly223=
XM_011535171.2:c.668G=	XP_011533473.1:p.Gly223=
XR_002957522.1:n.137C=
NM_000321.3:c.929G= MANE Select	NP_000312.2:p.Gly310=