Canonical Allele Identifier: CA388163367

Gene: RB1

Linked Data

• dbSNP Id: rs1555286684
• MyVariant Identifiers: chr13:g.48955410G>A (hg19) ; chr13:g.48381274G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48381274G>A , CM000675.2:g.48381274G>A	GRCh38
NC_000013.10:g.48955410G>A , CM000675.1:g.48955410G>A	GRCh37
NC_000013.9:g.47853411G>A	NCBI36
NG_009009.1:g.82528G>A , LRG_517:g.82528G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1526G>A MANE Select	ENSP00000267163.4:p.Gly509Glu
ENST00000643064.1:c.25G>A
ENST00000650461.1:c.1526G>A	ENSP00000497193.1:p.Gly509Glu
ENST00000267163.4:c.1526G>A	ENSP00000267163.4:p.Gly509Glu
NM_000321.2:c.1526G>A , LRG_517t1:c.1526G>A	NP_000312.2:p.Gly509Glu
XM_011535171.1:c.1265G>A	XP_011533473.1:p.Gly422Glu
XM_011535171.2:c.1265G>A	XP_011533473.1:p.Gly422Glu
NM_000321.3:c.1526G>A MANE Select	NP_000312.2:p.Gly509Glu