Canonical Allele Identifier: CA408014169

Gene: SNRPB

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2463205C>T , CM000682.2:g.2463205C>T	GRCh38
NC_000020.10:g.2443851C>T , CM000682.1:g.2443851C>T	GRCh37
NC_000020.9:g.2391851C>T	NCBI36
NG_042057.1:g.12649G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688423.1:n.2846G>A
ENST00000688450.1:n.1523G>A
ENST00000688775.1:n.2327G>A
ENST00000689440.1:n.2038G>A
ENST00000689611.1:n.1692G>A
ENST00000690623.1:n.616G>A
ENST00000693393.1:n.2329G>A
ENST00000381342.7:c.443G>A MANE Select	ENSP00000370746.3:p.Gly148Asp
ENST00000339610.10:c.443G>A	ENSP00000342305.7:p.Gly148Asp
ENST00000381342.6:c.443G>A	ENSP00000370746.2:p.Gly148Asp
ENST00000438552.6:c.443G>A	ENSP00000412566.2:p.Gly148Asp
ENST00000474384.2:c.*354G>A	ENSP00000474579.1:n.*354G>A
NM_003091.3:c.443G>A	NP_003082.1:p.Gly148Asp
NM_198216.1:c.443G>A	NP_937859.1:p.Gly148Asp
NM_003091.4:c.443G>A MANE Select	NP_003082.1:p.Gly148Asp
NM_198216.2:c.443G>A	NP_937859.1:p.Gly148Asp