Canonical Allele Identifier: CA2089967195

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48342544T= , CM000675.2:g.48342544T=	GRCh38
NC_000013.10:g.48916680T= , CM000675.1:g.48916680T=	GRCh37
NC_000013.9:g.47814681T=	NCBI36
NG_009009.1:g.43798T= , LRG_517:g.43798T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.265-55T= MANE Select	ENSP00000267163.4:n.265-55T=
ENST00000650461.1:c.265-55T=	ENSP00000497193.1:n.265-55T=
ENST00000267163.4:c.265-55T=	ENSP00000267163.4:n.265-55T=
ENST00000467505.5:c.138-17473T=	ENSP00000434702.1:n.138-17473T=
ENST00000525036.1:n.427-55T=
NM_000321.2:c.265-55T= , LRG_517t1:c.265-55T=	NP_000312.2:n.265-55T=
XM_011535171.1:c.4-55T=	XP_011533473.1:n.4-55T=
XM_011535171.2:c.4-55T=	XP_011533473.1:n.4-55T=
NM_000321.3:c.265-55T= MANE Select	NP_000312.2:n.265-55T=