Canonical Allele Identifier: CA2090008128

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48459788C= , CM000675.2:g.48459788C=	GRCh38
NC_000013.10:g.49033924C= , CM000675.1:g.49033924C=	GRCh37
NC_000013.9:g.47931925C=	NCBI36
NG_009009.1:g.161042C= , LRG_517:g.161042C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2061C= MANE Select	ENSP00000267163.4:p.Thr687=
ENST00000643064.1:c.194+78345C=
ENST00000650461.1:c.2061C=	ENSP00000497193.1:p.Thr687=
ENST00000267163.4:c.2061C=	ENSP00000267163.4:p.Thr687=
NM_000321.2:c.2061C= , LRG_517t1:c.2061C=	NP_000312.2:p.Thr687=
XM_011535171.1:c.1800C=	XP_011533473.1:p.Thr600=
XM_011535171.2:c.1800C=	XP_011533473.1:p.Thr600=
NM_000321.3:c.2061C= MANE Select	NP_000312.2:p.Thr687=