Canonical Allele Identifier: CA388163746
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48381357A>G , CM000675.2:g.48381357A>G GRCh38
NC_000013.10:g.48955493A>G , CM000675.1:g.48955493A>G GRCh37
NC_000013.9:g.47853494A>G NCBI36
NG_009009.1:g.82611A>G , LRG_517:g.82611A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1609A>G MANE Select ENSP00000267163.4:p.Lys537Glu
ENST00000643064.1:c.108A>G
ENST00000650461.1:c.1609A>G ENSP00000497193.1:p.Lys537Glu
ENST00000267163.4:c.1609A>G ENSP00000267163.4:p.Lys537Glu
NM_000321.2:c.1609A>G , LRG_517t1:c.1609A>G NP_000312.2:p.Lys537Glu
XM_011535171.1:c.1348A>G XP_011533473.1:p.Lys450Glu
XM_011535171.2:c.1348A>G XP_011533473.1:p.Lys450Glu
NM_000321.3:c.1609A>G MANE Select NP_000312.2:p.Lys537Glu