Canonical Allele Identifier: CA388168211

Gene: RB1

Linked Data

• dbSNP Id: rs2138358938
• MyVariant Identifiers: chr13:g.49050851C>A (hg19) ; chr13:g.48476715C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476715C>A , CM000675.2:g.48476715C>A	GRCh38
NC_000013.10:g.49050851C>A , CM000675.1:g.49050851C>A	GRCh37
NC_000013.9:g.47948852C>A	NCBI36
NG_009009.1:g.177969C>A , LRG_517:g.177969C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2535C>A MANE Select	ENSP00000267163.4:p.Phe845Leu
ENST00000643064.1:c.194+95272C>A
ENST00000650461.1:c.2535C>A	ENSP00000497193.1:p.Phe845Leu
ENST00000267163.4:c.2535C>A	ENSP00000267163.4:p.Phe845Leu
ENST00000484879.1:n.269C>A
ENST00000531171.5:n.138C>A
NM_000321.2:c.2535C>A , LRG_517t1:c.2535C>A	NP_000312.2:p.Phe845Leu
XM_011535171.1:c.2274C>A	XP_011533473.1:p.Phe758Leu
XM_011535171.2:c.2274C>A	XP_011533473.1:p.Phe758Leu
NM_000321.3:c.2535C>A MANE Select	NP_000312.2:p.Phe845Leu