Canonical Allele Identifier: CA2346122568

Gene: SNRPB

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2470705T= , CM000682.2:g.2470705T=	GRCh38
NC_000020.10:g.2451351T= , CM000682.1:g.2451351T=	GRCh37
NC_000020.9:g.2399351T=	NCBI36
NG_042057.1:g.5149A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688423.1:n.83A=
ENST00000688775.1:n.83A=
ENST00000689440.1:n.85A=
ENST00000690623.1:n.35A=
ENST00000693393.1:n.85A=
ENST00000381342.7:c.-15A= MANE Select	ENSP00000370746.3:n.-15A=
ENST00000339610.10:c.-15A=	ENSP00000342305.7:n.-15A=
ENST00000381342.6:c.-15A=	ENSP00000370746.2:n.-15A=
ENST00000438552.6:c.-15A=	ENSP00000412566.2:n.-15A=
ENST00000461548.1:c.305-2947A=	ENSP00000456213.1:n.305-2947A=
ENST00000474384.2:c.-15A=	ENSP00000474579.1:n.-15A=
NM_003091.3:c.-15A=	NP_003082.1:n.-15A=
NM_198216.1:c.-15A=	NP_937859.1:n.-15A=
NM_003091.4:c.-15A= MANE Select	NP_003082.1:n.-15A=
NM_198216.2:c.-15A=	NP_937859.1:n.-15A=