Canonical Allele Identifier: CA483726188

Gene: RB1

Linked Data

• MyVariant Identifiers: chr13:g.48916828C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48342692C>T , CM000675.2:g.48342692C>T	GRCh38
NC_000013.10:g.48916828C>T , CM000675.1:g.48916828C>T	GRCh37
NC_000013.9:g.47814829C>T	NCBI36
NG_009009.1:g.43946C>T , LRG_517:g.43946C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.358C>T MANE Select	ENSP00000267163.4:p.Leu120=
ENST00000650461.1:c.358C>T	ENSP00000497193.1:p.Leu120=
ENST00000267163.4:c.358C>T	ENSP00000267163.4:p.Leu120=
ENST00000467505.5:c.138-17325C>T	ENSP00000434702.1:n.138-17325C>T
ENST00000525036.1:n.520C>T
NM_000321.2:c.358C>T , LRG_517t1:c.358C>T	NP_000312.2:p.Leu120=
XM_011535171.1:c.97C>T	XP_011533473.1:p.Leu33=
XM_011535171.2:c.97C>T	XP_011533473.1:p.Leu33=
NM_000321.3:c.358C>T MANE Select	NP_000312.2:p.Leu120=