Canonical Allele Identifier: CA2090013912

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48452859C= , CM000675.2:g.48452859C=	GRCh38
NC_000013.10:g.49026995C= , CM000675.1:g.49026995C=	GRCh37
NC_000013.9:g.47924996C=	NCBI36
NG_009009.1:g.154113C= , LRG_517:g.154113C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.1696-134C= MANE Select	ENSP00000267163.4:n.1696-134C=
ENST00000643064.1:c.194+71416C=
ENST00000650461.1:c.1696-134C=	ENSP00000497193.1:n.1696-134C=
ENST00000267163.4:c.1696-134C=	ENSP00000267163.4:n.1696-134C=
ENST00000480491.1:n.395-134C=
NM_000321.2:c.1696-134C= , LRG_517t1:c.1696-134C=	NP_000312.2:n.1696-134C=
XM_011535171.1:c.1435-134C=	XP_011533473.1:n.1435-134C=
XM_011535171.2:c.1435-134C=	XP_011533473.1:n.1435-134C=
NM_000321.3:c.1696-134C= MANE Select	NP_000312.2:n.1696-134C=