Canonical Allele Identifier: CA2622977130
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303777C>A , CM000675.2:g.48303777C>A GRCh38
NC_000013.10:g.48877913C>A , CM000675.1:g.48877913C>A GRCh37
NC_000013.9:g.47775914C>A NCBI36
NG_009009.1:g.5031C>A , LRG_517:g.5031C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.-136C>A MANE Select ENSP00000267163.4:n.-136C>A
ENST00000646097.1:c.-136C>A ENSP00000496556.1:n.-136C>A
ENST00000650461.1:c.-136C>A ENSP00000497193.1:n.-136C>A
ENST00000267163.4:c.-136C>A ENSP00000267163.4:n.-136C>A
ENST00000467505.5:c.-136C>A ENSP00000434702.1:n.-136C>A
ENST00000525036.1:n.27C>A
NM_000321.2:c.-136C>A , LRG_517t1:c.-136C>A NP_000312.2:n.-136C>A
NM_000321.3:c.-136C>A MANE Select NP_000312.2:n.-136C>A