Canonical Allele Identifier: CA483559461

Gene: RB1

Linked Data

• MyVariant Identifiers: chr13:g.48955451T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48381315T>C , CM000675.2:g.48381315T>C	GRCh38
NC_000013.10:g.48955451T>C , CM000675.1:g.48955451T>C	GRCh37
NC_000013.9:g.47853452T>C	NCBI36
NG_009009.1:g.82569T>C , LRG_517:g.82569T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1567T>C MANE Select	ENSP00000267163.4:p.Leu523=
ENST00000643064.1:c.66T>C
ENST00000650461.1:c.1567T>C	ENSP00000497193.1:p.Leu523=
ENST00000267163.4:c.1567T>C	ENSP00000267163.4:p.Leu523=
NM_000321.2:c.1567T>C , LRG_517t1:c.1567T>C	NP_000312.2:p.Leu523=
XM_011535171.1:c.1306T>C	XP_011533473.1:p.Leu436=
XM_011535171.2:c.1306T>C	XP_011533473.1:p.Leu436=
NM_000321.3:c.1567T>C MANE Select	NP_000312.2:p.Leu523=