Canonical Allele Identifier: CA388166683
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459694G>T , CM000675.2:g.48459694G>T GRCh38
NC_000013.10:g.49033830G>T , CM000675.1:g.49033830G>T GRCh37
NC_000013.9:g.47931831G>T NCBI36
NG_009009.1:g.160948G>T , LRG_517:g.160948G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1967G>T MANE Select ENSP00000267163.4:p.Arg656Leu
ENST00000643064.1:c.194+78251G>T
ENST00000650461.1:c.1967G>T ENSP00000497193.1:p.Arg656Leu
ENST00000267163.4:c.1967G>T ENSP00000267163.4:p.Arg656Leu
NM_000321.2:c.1967G>T , LRG_517t1:c.1967G>T NP_000312.2:p.Arg656Leu
XM_011535171.1:c.1706G>T XP_011533473.1:p.Arg569Leu
XM_011535171.2:c.1706G>T XP_011533473.1:p.Arg569Leu
NM_000321.3:c.1967G>T MANE Select NP_000312.2:p.Arg656Leu