Canonical Allele Identifier: CA2577319633
Gene: SNRPB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470736A>T , CM000682.2:g.2470736A>T GRCh38
NC_000020.10:g.2451382A>T , CM000682.1:g.2451382A>T GRCh37
NC_000020.9:g.2399382A>T NCBI36
NG_042057.1:g.5118T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000688423.1:n.52T>A
ENST00000688775.1:n.52T>A
ENST00000689440.1:n.54T>A
ENST00000690623.1:n.4T>A
ENST00000693393.1:n.54T>A
ENST00000381342.7:c.-46T>A MANE Select ENSP00000370746.3:n.-46T>A
ENST00000339610.10:c.-46T>A ENSP00000342305.7:n.-46T>A
ENST00000381342.6:c.-46T>A ENSP00000370746.2:n.-46T>A
ENST00000438552.6:c.-46T>A ENSP00000412566.2:n.-46T>A
ENST00000461548.1:c.305-2978T>A ENSP00000456213.1:n.305-2978T>A
NM_003091.3:c.-46T>A NP_003082.1:n.-46T>A
NM_198216.1:c.-46T>A NP_937859.1:n.-46T>A
NM_003091.4:c.-46T>A MANE Select NP_003082.1:n.-46T>A
NM_198216.2:c.-46T>A NP_937859.1:n.-46T>A