Canonical Allele Identifier: CA388157668

Gene: RB1

Linked Data

• ClinVar Variation Id: 527935
• ClinVar RCV Id: RCV000632966
• dbSNP Id: rs1555295354
• MyVariant Identifiers: chr13:g.49050979G>A (hg19) ; chr13:g.48476843G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476843G>A , CM000675.2:g.48476843G>A	GRCh38
NC_000013.10:g.49050979G>A , CM000675.1:g.49050979G>A	GRCh37
NC_000013.9:g.47948980G>A	NCBI36
NG_009009.1:g.178097G>A , LRG_517:g.178097G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2663G>A MANE Select	ENSP00000267163.4:p.Ser888Asn
ENST00000643064.1:c.194+95400G>A
ENST00000650461.1:c.2663G>A	ENSP00000497193.1:p.Ser888Asn
ENST00000267163.4:c.2663G>A	ENSP00000267163.4:p.Ser888Asn
ENST00000484879.1:n.397G>A
ENST00000531171.5:n.266G>A
NM_000321.2:c.2663G>A , LRG_517t1:c.2663G>A	NP_000312.2:p.Ser888Asn
XM_011535171.1:c.2402G>A	XP_011533473.1:p.Ser801Asn
XM_011535171.2:c.2402G>A	XP_011533473.1:p.Ser801Asn
NM_000321.3:c.2663G>A MANE Select	NP_000312.2:p.Ser888Asn