Canonical Allele Identifier: CA2089949669

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303857G= , CM000675.2:g.48303857G=	GRCh38
NC_000013.10:g.48877993G= , CM000675.1:g.48877993G=	GRCh37
NC_000013.9:g.47775994G=	NCBI36
NG_009009.1:g.5111G= , LRG_517:g.5111G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.-56G= MANE Select	ENSP00000267163.4:n.-56G=
ENST00000646097.1:c.-56G=	ENSP00000496556.1:n.-56G=
ENST00000650461.1:c.-56G=	ENSP00000497193.1:n.-56G=
ENST00000267163.4:c.-56G=	ENSP00000267163.4:n.-56G=
ENST00000467505.5:c.-56G=	ENSP00000434702.1:n.-56G=
ENST00000525036.1:n.107G=
NM_000321.2:c.-56G= , LRG_517t1:c.-56G=	NP_000312.2:n.-56G=
NM_000321.3:c.-56G= MANE Select	NP_000312.2:n.-56G=