Canonical Allele Identifier: CA388163381

Gene: RB1

Linked Data

• dbSNP Id: rs2138144966
• gnomAD v4: 13-48381277-C-T
• MyVariant Identifiers: chr13:g.48955413C>T (hg19) ; chr13:g.48381277C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48381277C>T , CM000675.2:g.48381277C>T	GRCh38
NC_000013.10:g.48955413C>T , CM000675.1:g.48955413C>T	GRCh37
NC_000013.9:g.47853414C>T	NCBI36
NG_009009.1:g.82531C>T , LRG_517:g.82531C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1529C>T MANE Select	ENSP00000267163.4:p.Thr510Ile
ENST00000643064.1:c.28C>T
ENST00000650461.1:c.1529C>T	ENSP00000497193.1:p.Thr510Ile
ENST00000267163.4:c.1529C>T	ENSP00000267163.4:p.Thr510Ile
NM_000321.2:c.1529C>T , LRG_517t1:c.1529C>T	NP_000312.2:p.Thr510Ile
XM_011535171.1:c.1268C>T	XP_011533473.1:p.Thr423Ile
XM_011535171.2:c.1268C>T	XP_011533473.1:p.Thr423Ile
NM_000321.3:c.1529C>T MANE Select	NP_000312.2:p.Thr510Ile