Canonical Allele Identifier: CA388250359

Gene: RB1

Linked Data

• dbSNP Id: rs2138027915
• MyVariant Identifiers: chr13:g.48878163C>G (hg19) ; chr13:g.48304027C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48304027C>G , CM000675.2:g.48304027C>G	GRCh38
NC_000013.10:g.48878163C>G , CM000675.1:g.48878163C>G	GRCh37
NC_000013.9:g.47776164C>G	NCBI36
NG_009009.1:g.5281C>G , LRG_517:g.5281C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.115C>G MANE Select	ENSP00000267163.4:p.Pro39Ala
ENST00000646097.1:c.115C>G	ENSP00000496556.1:p.Pro39Ala
ENST00000650461.1:c.115C>G	ENSP00000497193.1:p.Pro39Ala
ENST00000267163.4:c.115C>G	ENSP00000267163.4:p.Pro39Ala
ENST00000467505.5:c.115C>G	ENSP00000434702.1:p.Pro39Ala
ENST00000525036.1:n.277C>G
NM_000321.2:c.115C>G , LRG_517t1:c.115C>G	NP_000312.2:p.Pro39Ala
NM_000321.3:c.115C>G MANE Select	NP_000312.2:p.Pro39Ala