Canonical Allele Identifier: CA2089949505
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303747G= , CM000675.2:g.48303747G= GRCh38
NC_000013.10:g.48877883G= , CM000675.1:g.48877883G= GRCh37
NC_000013.9:g.47775884G= NCBI36
NG_009009.1:g.5001G= , LRG_517:g.5001G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646097.1:c.-166G= ENSP00000496556.1:n.-166G=
ENST00000650461.1:c.-166G= ENSP00000497193.1:n.-166G=
NM_000321.2:c.-166G= , LRG_517t1:c.-166G= NP_000312.2:n.-166G=