Canonical Allele Identifier: CA2346122669
Gene: SNRPB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470810C= , CM000682.2:g.2470810C= GRCh38
NC_000020.10:g.2451456C= , CM000682.1:g.2451456C= GRCh37
NC_000020.9:g.2399456C= NCBI36
NG_042057.1:g.5044G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339610.10:c.-120G= ENSP00000342305.7:n.-120G=
ENST00000381342.6:c.-120G= ENSP00000370746.2:n.-120G=
ENST00000438552.6:c.-120G= ENSP00000412566.2:n.-120G=
ENST00000461548.1:c.305-3052G= ENSP00000456213.1:n.305-3052G=
NM_003091.3:c.-120G= NP_003082.1:n.-120G=
NM_198216.1:c.-120G= NP_937859.1:n.-120G=