Canonical Allele Identifier: CA2090020992

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476599C= , CM000675.2:g.48476599C=	GRCh38
NC_000013.10:g.49050735C= , CM000675.1:g.49050735C=	GRCh37
NC_000013.9:g.47948736C=	NCBI36
NG_009009.1:g.177853C= , LRG_517:g.177853C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2521-102C= MANE Select	ENSP00000267163.4:n.2521-102C=
ENST00000643064.1:c.194+95156C=
ENST00000650461.1:c.2521-102C=	ENSP00000497193.1:n.2521-102C=
ENST00000267163.4:c.2521-102C=	ENSP00000267163.4:n.2521-102C=
ENST00000484879.1:n.153C=
ENST00000531171.5:n.123+77C=
NM_000321.2:c.2521-102C= , LRG_517t1:c.2521-102C=	NP_000312.2:n.2521-102C=
XM_011535171.1:c.2260-102C=	XP_011533473.1:n.2260-102C=
XM_011535171.2:c.2260-102C=	XP_011533473.1:n.2260-102C=
NM_000321.3:c.2521-102C= MANE Select	NP_000312.2:n.2521-102C=