Canonical Allele Identifier: CA2089972257

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48348628C= , CM000675.2:g.48348628C=	GRCh38
NC_000013.10:g.48922764C= , CM000675.1:g.48922764C=	GRCh37
NC_000013.9:g.47820765C=	NCBI36
NG_009009.1:g.49882C= , LRG_517:g.49882C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.540-328C= MANE Select	ENSP00000267163.4:n.540-328C=
ENST00000650461.1:c.540-328C=	ENSP00000497193.1:n.540-328C=
ENST00000267163.4:c.540-328C=	ENSP00000267163.4:n.540-328C=
ENST00000467505.5:c.138-11389C=	ENSP00000434702.1:n.138-11389C=
ENST00000525036.1:n.702-328C=
NM_000321.2:c.540-328C= , LRG_517t1:c.540-328C=	NP_000312.2:n.540-328C=
XM_011535171.1:c.279-328C=	XP_011533473.1:n.279-328C=
XM_011535171.2:c.279-328C=	XP_011533473.1:n.279-328C=
NM_000321.3:c.540-328C= MANE Select	NP_000312.2:n.540-328C=