Canonical Allele Identifier: CA2089949523
Gene: RB1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303757C= , CM000675.2:g.48303757C= GRCh38
NC_000013.10:g.48877893C= , CM000675.1:g.48877893C= GRCh37
NC_000013.9:g.47775894C= NCBI36
NG_009009.1:g.5011C= , LRG_517:g.5011C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.-156C= MANE Select ENSP00000267163.4:n.-156C=
ENST00000646097.1:c.-156C= ENSP00000496556.1:n.-156C=
ENST00000650461.1:c.-156C= ENSP00000497193.1:n.-156C=
ENST00000525036.1:n.7C=
NM_000321.2:c.-156C= , LRG_517t1:c.-156C= NP_000312.2:n.-156C=
NM_000321.3:c.-156C= MANE Select NP_000312.2:n.-156C=
Search 100 bp 5'
Search 100 bp 3'