Canonical Allele Identifier: CA2089950051

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303958G= , CM000675.2:g.48303958G=	GRCh38
NC_000013.10:g.48878094G= , CM000675.1:g.48878094G=	GRCh37
NC_000013.9:g.47776095G=	NCBI36
NG_009009.1:g.5212G= , LRG_517:g.5212G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.46G= MANE Select	ENSP00000267163.4:p.Ala16=
ENST00000646097.1:c.46G=	ENSP00000496556.1:p.Ala16=
ENST00000650461.1:c.46G=	ENSP00000497193.1:p.Ala16=
ENST00000267163.4:c.46G=	ENSP00000267163.4:p.Ala16=
ENST00000467505.5:c.46G=	ENSP00000434702.1:p.Ala16=
ENST00000525036.1:n.208G=
NM_000321.2:c.46G= , LRG_517t1:c.46G=	NP_000312.2:p.Ala16=
NM_000321.3:c.46G= MANE Select	NP_000312.2:p.Ala16=