Canonical Allele Identifier: CA2090019305

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48459417A= , CM000675.2:g.48459417A=	GRCh38
NC_000013.10:g.49033553A= , CM000675.1:g.49033553A=	GRCh37
NC_000013.9:g.47931554A=	NCBI36
NG_009009.1:g.160671A= , LRG_517:g.160671A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1961-271A= MANE Select	ENSP00000267163.4:n.1961-271A=
ENST00000643064.1:c.194+77974A=
ENST00000650461.1:c.1961-271A=	ENSP00000497193.1:n.1961-271A=
ENST00000267163.4:c.1961-271A=	ENSP00000267163.4:n.1961-271A=
NM_000321.2:c.1961-271A= , LRG_517t1:c.1961-271A=	NP_000312.2:n.1961-271A=
XM_011535171.1:c.1700-271A=	XP_011533473.1:n.1700-271A=
XM_011535171.2:c.1700-271A=	XP_011533473.1:n.1700-271A=
NM_000321.3:c.1961-271A= MANE Select	NP_000312.2:n.1961-271A=