Canonical Allele Identifier: CA2346122662
Gene: SNRPB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470802A= , CM000682.2:g.2470802A= GRCh38
NC_000020.10:g.2451448A= , CM000682.1:g.2451448A= GRCh37
NC_000020.9:g.2399448A= NCBI36
NG_042057.1:g.5052T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339610.10:c.-112T= ENSP00000342305.7:n.-112T=
ENST00000381342.6:c.-112T= ENSP00000370746.2:n.-112T=
ENST00000438552.6:c.-112T= ENSP00000412566.2:n.-112T=
ENST00000461548.1:c.305-3044T= ENSP00000456213.1:n.305-3044T=
NM_003091.3:c.-112T= NP_003082.1:n.-112T=
NM_198216.1:c.-112T= NP_937859.1:n.-112T=