Canonical Allele Identifier: CA388166698
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459705C>A , CM000675.2:g.48459705C>A GRCh38
NC_000013.10:g.49033841C>A , CM000675.1:g.49033841C>A GRCh37
NC_000013.9:g.47931842C>A NCBI36
NG_009009.1:g.160959C>A , LRG_517:g.160959C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1978C>A MANE Select ENSP00000267163.4:p.Leu660Ile
ENST00000643064.1:c.194+78262C>A
ENST00000650461.1:c.1978C>A ENSP00000497193.1:p.Leu660Ile
ENST00000267163.4:c.1978C>A ENSP00000267163.4:p.Leu660Ile
NM_000321.2:c.1978C>A , LRG_517t1:c.1978C>A NP_000312.2:p.Leu660Ile
XM_011535171.1:c.1717C>A XP_011533473.1:p.Leu573Ile
XM_011535171.2:c.1717C>A XP_011533473.1:p.Leu573Ile
NM_000321.3:c.1978C>A MANE Select NP_000312.2:p.Leu660Ile