Canonical Allele Identifier: CA483561086

Gene: RB1

Linked Data

• ClinVar Variation Id: 3231229
• ClinVar RCV Id: RCV004525300
• dbSNP Id: rs2138359346
• MyVariant Identifiers: chr13:g.49050920T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476784T>A , CM000675.2:g.48476784T>A	GRCh38
NC_000013.10:g.49050920T>A , CM000675.1:g.49050920T>A	GRCh37
NC_000013.9:g.47948921T>A	NCBI36
NG_009009.1:g.178038T>A , LRG_517:g.178038T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2604T>A MANE Select	ENSP00000267163.4:p.Pro868=
ENST00000643064.1:c.194+95341T>A
ENST00000650461.1:c.2604T>A	ENSP00000497193.1:p.Pro868=
ENST00000267163.4:c.2604T>A	ENSP00000267163.4:p.Pro868=
ENST00000484879.1:n.338T>A
ENST00000531171.5:n.207T>A
NM_000321.2:c.2604T>A , LRG_517t1:c.2604T>A	NP_000312.2:p.Pro868=
XM_011535171.1:c.2343T>A	XP_011533473.1:p.Pro781=
XM_011535171.2:c.2343T>A	XP_011533473.1:p.Pro781=
NM_000321.3:c.2604T>A MANE Select	NP_000312.2:p.Pro868=