Canonical Allele Identifier: CA2728071410

Gene: RB1

Linked Data

• dbSNP Id: rs2138326861

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48452960A>T , CM000675.2:g.48452960A>T	GRCh38
NC_000013.10:g.49027096A>T , CM000675.1:g.49027096A>T	GRCh37
NC_000013.9:g.47925097A>T	NCBI36
NG_009009.1:g.154214A>T , LRG_517:g.154214A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.1696-33A>T MANE Select	ENSP00000267163.4:n.1696-33A>T
ENST00000643064.1:c.194+71517A>T
ENST00000650461.1:c.1696-33A>T	ENSP00000497193.1:n.1696-33A>T
ENST00000267163.4:c.1696-33A>T	ENSP00000267163.4:n.1696-33A>T
ENST00000480491.1:n.395-33A>T
NM_000321.2:c.1696-33A>T , LRG_517t1:c.1696-33A>T	NP_000312.2:n.1696-33A>T
XM_011535171.1:c.1435-33A>T	XP_011533473.1:n.1435-33A>T
XM_011535171.2:c.1435-33A>T	XP_011533473.1:n.1435-33A>T
NM_000321.3:c.1696-33A>T MANE Select	NP_000312.2:n.1696-33A>T