Canonical Allele Identifier: CA2728030351

Gene: RB1

Linked Data

• dbSNP Id: rs2138026432

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303817G>A , CM000675.2:g.48303817G>A	GRCh38
NC_000013.10:g.48877953G>A , CM000675.1:g.48877953G>A	GRCh37
NC_000013.9:g.47775954G>A	NCBI36
NG_009009.1:g.5071G>A , LRG_517:g.5071G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.-96G>A MANE Select	ENSP00000267163.4:n.-96G>A
ENST00000646097.1:c.-96G>A	ENSP00000496556.1:n.-96G>A
ENST00000650461.1:c.-96G>A	ENSP00000497193.1:n.-96G>A
ENST00000267163.4:c.-96G>A	ENSP00000267163.4:n.-96G>A
ENST00000467505.5:c.-96G>A	ENSP00000434702.1:n.-96G>A
ENST00000525036.1:n.67G>A
NM_000321.2:c.-96G>A , LRG_517t1:c.-96G>A	NP_000312.2:n.-96G>A
NM_000321.3:c.-96G>A MANE Select	NP_000312.2:n.-96G>A