Canonical Allele Identifier: CA2728087161

Gene: RB1

Linked Data

• dbSNP Id: rs2138360020

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476922T>A , CM000675.2:g.48476922T>A	GRCh38
NC_000013.10:g.49051058T>A , CM000675.1:g.49051058T>A	GRCh37
NC_000013.9:g.47949059T>A	NCBI36
NG_009009.1:g.178176T>A , LRG_517:g.178176T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2663+79T>A MANE Select	ENSP00000267163.4:n.2663+79T>A
ENST00000643064.1:c.194+95479T>A
ENST00000650461.1:c.2663+79T>A	ENSP00000497193.1:n.2663+79T>A
ENST00000267163.4:c.2663+79T>A	ENSP00000267163.4:n.2663+79T>A
ENST00000484879.1:n.397+79T>A
ENST00000531171.5:n.266+79T>A
NM_000321.2:c.2663+79T>A , LRG_517t1:c.2663+79T>A	NP_000312.2:n.2663+79T>A
XM_011535171.1:c.2402+79T>A	XP_011533473.1:n.2402+79T>A
XM_011535171.2:c.2402+79T>A	XP_011533473.1:n.2402+79T>A
NM_000321.3:c.2663+79T>A MANE Select	NP_000312.2:n.2663+79T>A