Canonical Allele Identifier: CA388157675

Gene: RB1

Linked Data

• ClinVar Variation Id: 1076418
• ClinVar RCV Id: RCV001390327
• dbSNP Id: rs2138359672
• MyVariant Identifiers: chr13:g.49050980G>T (hg19) ; chr13:g.48476844G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476844G>T , CM000675.2:g.48476844G>T	GRCh38
NC_000013.10:g.49050980G>T , CM000675.1:g.49050980G>T	GRCh37
NC_000013.9:g.47948981G>T	NCBI36
NG_009009.1:g.178098G>T , LRG_517:g.178098G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2663+1G>T MANE Select	ENSP00000267163.4:n.2663+1G>T
ENST00000643064.1:c.194+95401G>T
ENST00000650461.1:c.2663+1G>T	ENSP00000497193.1:n.2663+1G>T
ENST00000267163.4:c.2663+1G>T	ENSP00000267163.4:n.2663+1G>T
ENST00000484879.1:n.397+1G>T
ENST00000531171.5:n.266+1G>T
NM_000321.2:c.2663+1G>T , LRG_517t1:c.2663+1G>T	NP_000312.2:n.2663+1G>T
XM_011535171.1:c.2402+1G>T	XP_011533473.1:n.2402+1G>T
XM_011535171.2:c.2402+1G>T	XP_011533473.1:n.2402+1G>T
NM_000321.3:c.2663+1G>T MANE Select	NP_000312.2:n.2663+1G>T