Canonical Allele Identifier: CA2346122641

Gene: SNRPB

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2470779A= , CM000682.2:g.2470779A=	GRCh38
NC_000020.10:g.2451425A= , CM000682.1:g.2451425A=	GRCh37
NC_000020.9:g.2399425A=	NCBI36
NG_042057.1:g.5075T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000688423.1:n.9T=
ENST00000688775.1:n.9T=
ENST00000689440.1:n.11T=
ENST00000693393.1:n.11T=
ENST00000381342.7:c.-89T= MANE Select	ENSP00000370746.3:n.-89T=
ENST00000339610.10:c.-89T=	ENSP00000342305.7:n.-89T=
ENST00000381342.6:c.-89T=	ENSP00000370746.2:n.-89T=
ENST00000438552.6:c.-89T=	ENSP00000412566.2:n.-89T=
ENST00000461548.1:c.305-3021T=	ENSP00000456213.1:n.305-3021T=
NM_003091.3:c.-89T=	NP_003082.1:n.-89T=
NM_198216.1:c.-89T=	NP_937859.1:n.-89T=
NM_003091.4:c.-89T= MANE Select	NP_003082.1:n.-89T=
NM_198216.2:c.-89T=	NP_937859.1:n.-89T=