Canonical Allele Identifier: CA2090020996

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476603T= , CM000675.2:g.48476603T=	GRCh38
NC_000013.10:g.49050739T= , CM000675.1:g.49050739T=	GRCh37
NC_000013.9:g.47948740T=	NCBI36
NG_009009.1:g.177857T= , LRG_517:g.177857T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2521-98T= MANE Select	ENSP00000267163.4:n.2521-98T=
ENST00000643064.1:c.194+95160T=
ENST00000650461.1:c.2521-98T=	ENSP00000497193.1:n.2521-98T=
ENST00000267163.4:c.2521-98T=	ENSP00000267163.4:n.2521-98T=
ENST00000484879.1:n.157T=
ENST00000531171.5:n.123+81T=
NM_000321.2:c.2521-98T= , LRG_517t1:c.2521-98T=	NP_000312.2:n.2521-98T=
XM_011535171.1:c.2260-98T=	XP_011533473.1:n.2260-98T=
XM_011535171.2:c.2260-98T=	XP_011533473.1:n.2260-98T=
NM_000321.3:c.2521-98T= MANE Select	NP_000312.2:n.2521-98T=