Canonical Allele Identifier: CA2089972245

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48348613T= , CM000675.2:g.48348613T=	GRCh38
NC_000013.10:g.48922749T= , CM000675.1:g.48922749T=	GRCh37
NC_000013.9:g.47820750T=	NCBI36
NG_009009.1:g.49867T= , LRG_517:g.49867T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.540-343T= MANE Select	ENSP00000267163.4:n.540-343T=
ENST00000650461.1:c.540-343T=	ENSP00000497193.1:n.540-343T=
ENST00000267163.4:c.540-343T=	ENSP00000267163.4:n.540-343T=
ENST00000467505.5:c.138-11404T=	ENSP00000434702.1:n.138-11404T=
ENST00000525036.1:n.702-343T=
NM_000321.2:c.540-343T= , LRG_517t1:c.540-343T=	NP_000312.2:n.540-343T=
XM_011535171.1:c.279-343T=	XP_011533473.1:n.279-343T=
XM_011535171.2:c.279-343T=	XP_011533473.1:n.279-343T=
NM_000321.3:c.540-343T= MANE Select	NP_000312.2:n.540-343T=