Canonical Allele Identifier: CA388157639

Gene: RB1

Linked Data

• dbSNP Id: rs1460190600
• MyVariant Identifiers: chr13:g.49050972G>C (hg19) ; chr13:g.48476836G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476836G>C , CM000675.2:g.48476836G>C	GRCh38
NC_000013.10:g.49050972G>C , CM000675.1:g.49050972G>C	GRCh37
NC_000013.9:g.47948973G>C	NCBI36
NG_009009.1:g.178090G>C , LRG_517:g.178090G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2656G>C MANE Select	ENSP00000267163.4:p.Asp886His
ENST00000643064.1:c.194+95393G>C
ENST00000650461.1:c.2656G>C	ENSP00000497193.1:p.Asp886His
ENST00000267163.4:c.2656G>C	ENSP00000267163.4:p.Asp886His
ENST00000484879.1:n.390G>C
ENST00000531171.5:n.259G>C
NM_000321.2:c.2656G>C , LRG_517t1:c.2656G>C	NP_000312.2:p.Asp886His
XM_011535171.1:c.2395G>C	XP_011533473.1:p.Asp799His
XM_011535171.2:c.2395G>C	XP_011533473.1:p.Asp799His
NM_000321.3:c.2656G>C MANE Select	NP_000312.2:p.Asp886His