Canonical Allele Identifier: CA2090013582

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48464941T= , CM000675.2:g.48464941T=	GRCh38
NC_000013.10:g.49039077T= , CM000675.1:g.49039077T=	GRCh37
NC_000013.9:g.47937078T=	NCBI36
NG_009009.1:g.166195T= , LRG_517:g.166195T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.2212-57T= MANE Select	ENSP00000267163.4:n.2212-57T=
ENST00000643064.1:c.194+83498T=
ENST00000650461.1:c.2212-57T=	ENSP00000497193.1:n.2212-57T=
ENST00000267163.4:c.2212-57T=	ENSP00000267163.4:n.2212-57T=
NM_000321.2:c.2212-57T= , LRG_517t1:c.2212-57T=	NP_000312.2:n.2212-57T=
XM_011535171.1:c.1951-57T=	XP_011533473.1:n.1951-57T=
XM_011535171.2:c.1951-57T=	XP_011533473.1:n.1951-57T=
NM_000321.3:c.2212-57T= MANE Select	NP_000312.2:n.2212-57T=