Canonical Allele Identifier: CA388157531

Gene: RB1

Linked Data

• dbSNP Id: rs2138359484
• MyVariant Identifiers: chr13:g.49050946T>A (hg19) ; chr13:g.48476810T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476810T>A , CM000675.2:g.48476810T>A	GRCh38
NC_000013.10:g.49050946T>A , CM000675.1:g.49050946T>A	GRCh37
NC_000013.9:g.47948947T>A	NCBI36
NG_009009.1:g.178064T>A , LRG_517:g.178064T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2630T>A MANE Select	ENSP00000267163.4:p.Phe877Tyr
ENST00000643064.1:c.194+95367T>A
ENST00000650461.1:c.2630T>A	ENSP00000497193.1:p.Phe877Tyr
ENST00000267163.4:c.2630T>A	ENSP00000267163.4:p.Phe877Tyr
ENST00000484879.1:n.364T>A
ENST00000531171.5:n.233T>A
NM_000321.2:c.2630T>A , LRG_517t1:c.2630T>A	NP_000312.2:p.Phe877Tyr
XM_011535171.1:c.2369T>A	XP_011533473.1:p.Phe790Tyr
XM_011535171.2:c.2369T>A	XP_011533473.1:p.Phe790Tyr
NM_000321.3:c.2630T>A MANE Select	NP_000312.2:p.Phe877Tyr