Canonical Allele Identifier: CA388166743

Gene: RB1

Linked Data

• dbSNP Id: rs551747882
• MyVariant Identifiers: chr13:g.49033866G>C (hg19) ; chr13:g.48459730G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48459730G>C , CM000675.2:g.48459730G>C	GRCh38
NC_000013.10:g.49033866G>C , CM000675.1:g.49033866G>C	GRCh37
NC_000013.9:g.47931867G>C	NCBI36
NG_009009.1:g.160984G>C , LRG_517:g.160984G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2003G>C MANE Select	ENSP00000267163.4:p.Arg668Pro
ENST00000643064.1:c.194+78287G>C
ENST00000650461.1:c.2003G>C	ENSP00000497193.1:p.Arg668Pro
ENST00000267163.4:c.2003G>C	ENSP00000267163.4:p.Arg668Pro
NM_000321.2:c.2003G>C , LRG_517t1:c.2003G>C	NP_000312.2:p.Arg668Pro
XM_011535171.1:c.1742G>C	XP_011533473.1:p.Arg581Pro
XM_011535171.2:c.1742G>C	XP_011533473.1:p.Arg581Pro
NM_000321.3:c.2003G>C MANE Select	NP_000312.2:p.Arg668Pro