Canonical Allele Identifier: CA388168254

Gene: RB1

Linked Data

• ClinVar Variation Id: 577035
• ClinVar RCV Id: RCV000699688
• dbSNP Id: rs1566240932
• MyVariant Identifiers: chr13:g.49050868T>C (hg19) ; chr13:g.48476732T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476732T>C , CM000675.2:g.48476732T>C	GRCh38
NC_000013.10:g.49050868T>C , CM000675.1:g.49050868T>C	GRCh37
NC_000013.9:g.47948869T>C	NCBI36
NG_009009.1:g.177986T>C , LRG_517:g.177986T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2552T>C MANE Select	ENSP00000267163.4:p.Met851Thr
ENST00000643064.1:c.194+95289T>C
ENST00000650461.1:c.2552T>C	ENSP00000497193.1:p.Met851Thr
ENST00000267163.4:c.2552T>C	ENSP00000267163.4:p.Met851Thr
ENST00000484879.1:n.286T>C
ENST00000531171.5:n.155T>C
NM_000321.2:c.2552T>C , LRG_517t1:c.2552T>C	NP_000312.2:p.Met851Thr
XM_011535171.1:c.2291T>C	XP_011533473.1:p.Met764Thr
XM_011535171.2:c.2291T>C	XP_011533473.1:p.Met764Thr
NM_000321.3:c.2552T>C MANE Select	NP_000312.2:p.Met851Thr