Canonical Allele Identifier: CA2089949502
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303744G= , CM000675.2:g.48303744G= GRCh38
NC_000013.10:g.48877880G= , CM000675.1:g.48877880G= GRCh37
NC_000013.9:g.47775881G= NCBI36
NG_009009.1:g.4998G= , LRG_517:g.4998G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646097.1:c.-169G= ENSP00000496556.1:n.-169G=