Canonical Allele Identifier: CA2090013581

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48464938C= , CM000675.2:g.48464938C=	GRCh38
NC_000013.10:g.49039074C= , CM000675.1:g.49039074C=	GRCh37
NC_000013.9:g.47937075C=	NCBI36
NG_009009.1:g.166192C= , LRG_517:g.166192C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.2212-60C= MANE Select	ENSP00000267163.4:n.2212-60C=
ENST00000643064.1:c.194+83495C=
ENST00000650461.1:c.2212-60C=	ENSP00000497193.1:n.2212-60C=
ENST00000267163.4:c.2212-60C=	ENSP00000267163.4:n.2212-60C=
NM_000321.2:c.2212-60C= , LRG_517t1:c.2212-60C=	NP_000312.2:n.2212-60C=
XM_011535171.1:c.1951-60C=	XP_011533473.1:n.1951-60C=
XM_011535171.2:c.1951-60C=	XP_011533473.1:n.1951-60C=
NM_000321.3:c.2212-60C= MANE Select	NP_000312.2:n.2212-60C=