Canonical Allele Identifier: CA2651630538

Gene: SNRPB

Linked Data

• gnomAD v4: 20-2470795-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2470795_2470796insT , CM000682.2:g.2470795_2470796insT	GRCh38
NC_000020.10:g.2451441_2451442insT , CM000682.1:g.2451441_2451442insT	GRCh37
NC_000020.9:g.2399441_2399442insT	NCBI36
NG_042057.1:g.5058_5059insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339610.10:c.-106_-105insA	ENSP00000342305.7:n.-106_-105insA
ENST00000381342.6:c.-106_-105insA	ENSP00000370746.2:n.-106_-105insA
ENST00000438552.6:c.-106_-105insA	ENSP00000412566.2:n.-106_-105insA
ENST00000461548.1:c.305-3038_305-3037insA	ENSP00000456213.1:n.305-3038_305-3037insA
NM_003091.3:c.-106_-105insA	NP_003082.1:n.-106_-105insA
NM_198216.1:c.-106_-105insA	NP_937859.1:n.-106_-105insA