Canonical Allele Identifier: CA2089972425
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48381322C= , CM000675.2:g.48381322C= GRCh38
NC_000013.10:g.48955458C= , CM000675.1:g.48955458C= GRCh37
NC_000013.9:g.47853459C= NCBI36
NG_009009.1:g.82576C= , LRG_517:g.82576C=

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1574C= MANE Select ENSP00000267163.4:p.Ala525=
ENST00000643064.1:c.73C=
ENST00000650461.1:c.1574C= ENSP00000497193.1:p.Ala525=
ENST00000267163.4:c.1574C= ENSP00000267163.4:p.Ala525=
NM_000321.2:c.1574C= , LRG_517t1:c.1574C= NP_000312.2:p.Ala525=
XM_011535171.1:c.1313C= XP_011533473.1:p.Ala438=
XM_011535171.2:c.1313C= XP_011533473.1:p.Ala438=
NM_000321.3:c.1574C= MANE Select NP_000312.2:p.Ala525=