Canonical Allele Identifier: CA2090019384

Gene: RB1

Linked Data

• dbSNP Id: rs1949382325

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48459531_48459532insC , CM000675.2:g.48459531_48459532insC	GRCh38
NC_000013.10:g.49033667_49033668insC , CM000675.1:g.49033667_49033668insC	GRCh37
NC_000013.9:g.47931668_47931669insC	NCBI36
NG_009009.1:g.160785_160786insC , LRG_517:g.160785_160786insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1961-157_1961-156insC MANE Select	ENSP00000267163.4:n.1961-157_1961-156insC
ENST00000643064.1:c.194+78088_194+78089insC
ENST00000650461.1:c.1961-157_1961-156insC	ENSP00000497193.1:n.1961-157_1961-156insC
ENST00000267163.4:c.1961-157_1961-156insC	ENSP00000267163.4:n.1961-157_1961-156insC
NM_000321.2:c.1961-157_1961-156insC , LRG_517t1:c.1961-157_1961-156insC	NP_000312.2:n.1961-157_1961-156insC
XM_011535171.1:c.1700-157_1700-156insC	XP_011533473.1:n.1700-157_1700-156insC
XM_011535171.2:c.1700-157_1700-156insC	XP_011533473.1:n.1700-157_1700-156insC
NM_000321.3:c.1961-157_1961-156insC MANE Select	NP_000312.2:n.1961-157_1961-156insC