Canonical Allele Identifier: CA14803586

Gene: SNRPB

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2462470G>A , CM000682.2:g.2462470G>A	GRCh38
NC_000020.10:g.2443116G>A , CM000682.1:g.2443116G>A	GRCh37
NC_000020.9:g.2391116G>A	NCBI36
NG_042057.1:g.13384C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688423.1:n.3254C>T
ENST00000688450.1:n.1765+166C>T
ENST00000688775.1:n.2569+166C>T
ENST00000689440.1:n.2280+166C>T
ENST00000689611.1:n.2100C>T
ENST00000690623.1:n.1024C>T
ENST00000693393.1:n.2737C>T
ENST00000381342.7:c.685+166C>T MANE Select	ENSP00000370746.3:n.685+166C>T
ENST00000339610.10:c.684+166C>T	ENSP00000342305.7:n.684+166C>T
ENST00000381342.6:c.685+166C>T	ENSP00000370746.2:n.685+166C>T
ENST00000438552.6:c.685+166C>T	ENSP00000412566.2:n.685+166C>T
ENST00000474384.2:c.*596+166C>T	ENSP00000474579.1:n.*596+166C>T
NM_003091.3:c.685+166C>T	NP_003082.1:n.685+166C>T
NM_198216.1:c.685+166C>T	NP_937859.1:n.685+166C>T
NM_003091.4:c.685+166C>T MANE Select	NP_003082.1:n.685+166C>T
NM_198216.2:c.685+166C>T	NP_937859.1:n.685+166C>T