Canonical Allele Identifier: CA2622977171
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs925207403

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303815G>T , CM000675.2:g.48303815G>T GRCh38
NC_000013.10:g.48877951G>T , CM000675.1:g.48877951G>T GRCh37
NC_000013.9:g.47775952G>T NCBI36
NG_009009.1:g.5069G>T , LRG_517:g.5069G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.-98G>T MANE Select ENSP00000267163.4:n.-98G>T
ENST00000646097.1:c.-98G>T ENSP00000496556.1:n.-98G>T
ENST00000650461.1:c.-98G>T ENSP00000497193.1:n.-98G>T
ENST00000267163.4:c.-98G>T ENSP00000267163.4:n.-98G>T
ENST00000467505.5:c.-98G>T ENSP00000434702.1:n.-98G>T
ENST00000525036.1:n.65G>T
NM_000321.2:c.-98G>T , LRG_517t1:c.-98G>T NP_000312.2:n.-98G>T
NM_000321.3:c.-98G>T MANE Select NP_000312.2:n.-98G>T