Canonical Allele Identifier: CA388162900

Gene: RB1

Linked Data

• COSMIC: COSM6042749 ; COSM6042750
• MyVariant Identifiers: chr13:g.48954365G>A (hg19) ; chr13:g.48380229G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48380229G>A , CM000675.2:g.48380229G>A	GRCh38
NC_000013.10:g.48954365G>A , CM000675.1:g.48954365G>A	GRCh37
NC_000013.9:g.47852366G>A	NCBI36
NG_009009.1:g.81483G>A , LRG_517:g.81483G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.1486G>A MANE Select	ENSP00000267163.4:p.Ala496Thr
ENST00000650461.1:c.1486G>A	ENSP00000497193.1:p.Ala496Thr
ENST00000267163.4:c.1486G>A	ENSP00000267163.4:p.Ala496Thr
NM_000321.2:c.1486G>A , LRG_517t1:c.1486G>A	NP_000312.2:p.Ala496Thr
XM_011535171.1:c.1225G>A	XP_011533473.1:p.Ala409Thr
XM_011535171.2:c.1225G>A	XP_011533473.1:p.Ala409Thr
NM_000321.3:c.1486G>A MANE Select	NP_000312.2:p.Ala496Thr