Canonical Allele Identifier: CA657262529

Gene: SNRPB

Linked Data

• COSMIC: COSN20079749

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2470717_2470718insA , CM000682.2:g.2470717_2470718insA	GRCh38
NC_000020.10:g.2451363_2451364insA , CM000682.1:g.2451363_2451364insA	GRCh37
NC_000020.9:g.2399363_2399364insA	NCBI36
NG_042057.1:g.5136_5137insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688423.1:n.70_71insT
ENST00000688775.1:n.70_71insT
ENST00000689440.1:n.72_73insT
ENST00000690623.1:n.22_23insT
ENST00000693393.1:n.72_73insT
ENST00000381342.7:c.-28_-27insT MANE Select	ENSP00000370746.3:n.-28_-27insT
ENST00000339610.10:c.-28_-27insT	ENSP00000342305.7:n.-28_-27insT
ENST00000381342.6:c.-28_-27insT	ENSP00000370746.2:n.-28_-27insT
ENST00000438552.6:c.-28_-27insT	ENSP00000412566.2:n.-28_-27insT
ENST00000461548.1:c.305-2960_305-2959insT	ENSP00000456213.1:n.305-2960_305-2959insT
ENST00000474384.2:c.-28_-27insT	ENSP00000474579.1:n.-28_-27insT
NM_003091.3:c.-28_-27insT	NP_003082.1:n.-28_-27insT
NM_198216.1:c.-28_-27insT	NP_937859.1:n.-28_-27insT
NM_003091.4:c.-28_-27insT MANE Select	NP_003082.1:n.-28_-27insT
NM_198216.2:c.-28_-27insT	NP_937859.1:n.-28_-27insT