Canonical Allele Identifier: CA2089983401

Gene: RB1

Linked Data

• dbSNP Id: rs1952714200

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48367437_48367438del , CM000675.2:g.48367437_48367438del	GRCh38
NC_000013.10:g.48941573_48941574del , CM000675.1:g.48941573_48941574del	GRCh37
NC_000013.9:g.47839574_47839575del	NCBI36
NG_009009.1:g.68691_68692del , LRG_517:g.68691_68692del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.940-57_940-56del MANE Select	ENSP00000267163.4:n.940-57_940-56del
ENST00000650461.1:c.940-57_940-56del	ENSP00000497193.1:n.940-57_940-56del
ENST00000267163.4:c.940-57_940-56del	ENSP00000267163.4:n.940-57_940-56del
NM_000321.2:c.940-57_940-56del , LRG_517t1:c.940-57_940-56del	NP_000312.2:n.940-57_940-56del
XM_011535171.1:c.679-57_679-56del	XP_011533473.1:n.679-57_679-56del
XM_011535171.2:c.679-57_679-56del	XP_011533473.1:n.679-57_679-56del
XR_002957522.1:n.122-2458_122-2457del
NM_000321.3:c.940-57_940-56del MANE Select	NP_000312.2:n.940-57_940-56del