Canonical Allele Identifier: CA2089972439

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48381329T= , CM000675.2:g.48381329T=	GRCh38
NC_000013.10:g.48955465T= , CM000675.1:g.48955465T=	GRCh37
NC_000013.9:g.47853466T=	NCBI36
NG_009009.1:g.82583T= , LRG_517:g.82583T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1581T= MANE Select	ENSP00000267163.4:p.Asp527=
ENST00000643064.1:c.80T=
ENST00000650461.1:c.1581T=	ENSP00000497193.1:p.Asp527=
ENST00000267163.4:c.1581T=	ENSP00000267163.4:p.Asp527=
NM_000321.2:c.1581T= , LRG_517t1:c.1581T=	NP_000312.2:p.Asp527=
XM_011535171.1:c.1320T=	XP_011533473.1:p.Asp440=
XM_011535171.2:c.1320T=	XP_011533473.1:p.Asp440=
NM_000321.3:c.1581T= MANE Select	NP_000312.2:p.Asp527=