Canonical Allele Identifier: CA388157021

Gene: RB1

Linked Data

• ClinVar Variation Id: 1459669
• ClinVar RCV Id: RCV001959117 ; RCV002352655
• dbSNP Id: rs587776789
• MyVariant Identifiers: chr13:g.48923160G>C (hg19) ; chr13:g.48349024G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48349024G>C , CM000675.2:g.48349024G>C	GRCh38
NC_000013.10:g.48923160G>C , CM000675.1:g.48923160G>C	GRCh37
NC_000013.9:g.47821161G>C	NCBI36
NG_009009.1:g.50278G>C , LRG_517:g.50278G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.607+1G>C MANE Select	ENSP00000267163.4:n.607+1G>C
ENST00000650461.1:c.607+1G>C	ENSP00000497193.1:n.607+1G>C
ENST00000267163.4:c.607+1G>C	ENSP00000267163.4:n.607+1G>C
ENST00000467505.5:c.138-10993G>C	ENSP00000434702.1:n.138-10993G>C
ENST00000525036.1:n.769+1G>C
NM_000321.2:c.607+1G>C , LRG_517t1:c.607+1G>C	NP_000312.2:n.607+1G>C
XM_011535171.1:c.346+1G>C	XP_011533473.1:n.346+1G>C
XM_011535171.2:c.346+1G>C	XP_011533473.1:n.346+1G>C
NM_000321.3:c.607+1G>C MANE Select	NP_000312.2:n.607+1G>C