Canonical Allele Identifier: CA2573149589
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1692379
ClinVar RCV Id: RCV002255896
dbSNP Id: rs2138335800

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459690dup , CM000675.2:g.48459690dup GRCh38
NC_000013.10:g.49033826dup , CM000675.1:g.49033826dup GRCh37
NC_000013.9:g.47931827dup NCBI36
NG_009009.1:g.160944dup , LRG_517:g.160944dup

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1963dup MANE Select ENSP00000267163.4:p.Tyr655LeufsTer13
ENST00000643064.1:c.194+78247dup
ENST00000650461.1:c.1963dup ENSP00000497193.1:p.Tyr655LeufsTer13
ENST00000267163.4:c.1963dup ENSP00000267163.4:p.Tyr655LeufsTer13
NM_000321.2:c.1963dup , LRG_517t1:c.1963dup NP_000312.2:p.Tyr655LeufsTer13
XM_011535171.1:c.1702dup XP_011533473.1:p.Tyr568LeufsTer13
XM_011535171.2:c.1702dup XP_011533473.1:p.Tyr568LeufsTer13
NM_000321.3:c.1963dup MANE Select NP_000312.2:p.Tyr655LeufsTer13