Canonical Allele Identifier: CA2090021065

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476782C= , CM000675.2:g.48476782C=	GRCh38
NC_000013.10:g.49050918C= , CM000675.1:g.49050918C=	GRCh37
NC_000013.9:g.47948919C=	NCBI36
NG_009009.1:g.178036C= , LRG_517:g.178036C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2602C= MANE Select	ENSP00000267163.4:p.Pro868=
ENST00000643064.1:c.194+95339C=
ENST00000650461.1:c.2602C=	ENSP00000497193.1:p.Pro868=
ENST00000267163.4:c.2602C=	ENSP00000267163.4:p.Pro868=
ENST00000484879.1:n.336C=
ENST00000531171.5:n.205C=
NM_000321.2:c.2602C= , LRG_517t1:c.2602C=	NP_000312.2:p.Pro868=
XM_011535171.1:c.2341C=	XP_011533473.1:p.Pro781=
XM_011535171.2:c.2341C=	XP_011533473.1:p.Pro781=
NM_000321.3:c.2602C= MANE Select	NP_000312.2:p.Pro868=