Canonical Allele Identifier: CA483561106

Gene: RB1

Linked Data

• MyVariant Identifiers: chr13:g.49050953T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476817T>C , CM000675.2:g.48476817T>C	GRCh38
NC_000013.10:g.49050953T>C , CM000675.1:g.49050953T>C	GRCh37
NC_000013.9:g.47948954T>C	NCBI36
NG_009009.1:g.178071T>C , LRG_517:g.178071T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2637T>C MANE Select	ENSP00000267163.4:p.Ile879=
ENST00000643064.1:c.194+95374T>C
ENST00000650461.1:c.2637T>C	ENSP00000497193.1:p.Ile879=
ENST00000267163.4:c.2637T>C	ENSP00000267163.4:p.Ile879=
ENST00000484879.1:n.371T>C
ENST00000531171.5:n.240T>C
NM_000321.2:c.2637T>C , LRG_517t1:c.2637T>C	NP_000312.2:p.Ile879=
XM_011535171.1:c.2376T>C	XP_011533473.1:p.Ile792=
XM_011535171.2:c.2376T>C	XP_011533473.1:p.Ile792=
NM_000321.3:c.2637T>C MANE Select	NP_000312.2:p.Ile879=