Canonical Allele Identifier: CA483711580

Gene: RB1

Linked Data

• MyVariant Identifiers: chr13:g.48878075G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303939G>C , CM000675.2:g.48303939G>C	GRCh38
NC_000013.10:g.48878075G>C , CM000675.1:g.48878075G>C	GRCh37
NC_000013.9:g.47776076G>C	NCBI36
NG_009009.1:g.5193G>C , LRG_517:g.5193G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.27G>C MANE Select	ENSP00000267163.4:p.Thr9=
ENST00000646097.1:c.27G>C	ENSP00000496556.1:p.Thr9=
ENST00000650461.1:c.27G>C	ENSP00000497193.1:p.Thr9=
ENST00000267163.4:c.27G>C	ENSP00000267163.4:p.Thr9=
ENST00000467505.5:c.27G>C	ENSP00000434702.1:p.Thr9=
ENST00000525036.1:n.189G>C
NM_000321.2:c.27G>C , LRG_517t1:c.27G>C	NP_000312.2:p.Thr9=
NM_000321.3:c.27G>C MANE Select	NP_000312.2:p.Thr9=