Canonical Allele Identifier: CA388161252

Gene: RB1

Linked Data

• MyVariant Identifiers: chr13:g.48942707A>G (hg19) ; chr13:g.48368571A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48368571A>G , CM000675.2:g.48368571A>G	GRCh38
NC_000013.10:g.48942707A>G , CM000675.1:g.48942707A>G	GRCh37
NC_000013.9:g.47840708A>G	NCBI36
NG_009009.1:g.69825A>G , LRG_517:g.69825A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1094A>G MANE Select	ENSP00000267163.4:p.Glu365Gly
ENST00000650461.1:c.1094A>G	ENSP00000497193.1:p.Glu365Gly
ENST00000267163.4:c.1094A>G	ENSP00000267163.4:p.Glu365Gly
NM_000321.2:c.1094A>G , LRG_517t1:c.1094A>G	NP_000312.2:p.Glu365Gly
XM_011535171.1:c.833A>G	XP_011533473.1:p.Glu278Gly
XM_011535171.2:c.833A>G	XP_011533473.1:p.Glu278Gly
XR_002957522.1:n.122-3595T>C
NM_000321.3:c.1094A>G MANE Select	NP_000312.2:p.Glu365Gly