Canonical Allele Identifier: CA2090021105

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476870A= , CM000675.2:g.48476870A=	GRCh38
NC_000013.10:g.49051006A= , CM000675.1:g.49051006A=	GRCh37
NC_000013.9:g.47949007A=	NCBI36
NG_009009.1:g.178124A= , LRG_517:g.178124A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2663+27A= MANE Select	ENSP00000267163.4:n.2663+27A=
ENST00000643064.1:c.194+95427A=
ENST00000650461.1:c.2663+27A=	ENSP00000497193.1:n.2663+27A=
ENST00000267163.4:c.2663+27A=	ENSP00000267163.4:n.2663+27A=
ENST00000484879.1:n.397+27A=
ENST00000531171.5:n.266+27A=
NM_000321.2:c.2663+27A= , LRG_517t1:c.2663+27A=	NP_000312.2:n.2663+27A=
XM_011535171.1:c.2402+27A=	XP_011533473.1:n.2402+27A=
XM_011535171.2:c.2402+27A=	XP_011533473.1:n.2402+27A=
NM_000321.3:c.2663+27A= MANE Select	NP_000312.2:n.2663+27A=