Canonical Allele Identifier: CA2089969352
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48345011G= , CM000675.2:g.48345011G= GRCh38
NC_000013.10:g.48919147G= , CM000675.1:g.48919147G= GRCh37
NC_000013.9:g.47817148G= NCBI36
NG_009009.1:g.46265G= , LRG_517:g.46265G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.381-69G= MANE Select ENSP00000267163.4:n.381-69G=
ENST00000650461.1:c.381-69G= ENSP00000497193.1:n.381-69G=
ENST00000267163.4:c.381-69G= ENSP00000267163.4:n.381-69G=
ENST00000467505.5:c.138-15006G= ENSP00000434702.1:n.138-15006G=
ENST00000525036.1:n.543-69G=
NM_000321.2:c.381-69G= , LRG_517t1:c.381-69G= NP_000312.2:n.381-69G=
XM_011535171.1:c.120-69G= XP_011533473.1:n.120-69G=
XM_011535171.2:c.120-69G= XP_011533473.1:n.120-69G=
NM_000321.3:c.381-69G= MANE Select NP_000312.2:n.381-69G=