Canonical Allele Identifier: CA2346122629
Gene: SNRPB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470764T= , CM000682.2:g.2470764T= GRCh38
NC_000020.10:g.2451410T= , CM000682.1:g.2451410T= GRCh37
NC_000020.9:g.2399410T= NCBI36
NG_042057.1:g.5090A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000688423.1:n.24A=
ENST00000688775.1:n.24A=
ENST00000689440.1:n.26A=
ENST00000693393.1:n.26A=
ENST00000381342.7:c.-74A= MANE Select ENSP00000370746.3:n.-74A=
ENST00000339610.10:c.-74A= ENSP00000342305.7:n.-74A=
ENST00000381342.6:c.-74A= ENSP00000370746.2:n.-74A=
ENST00000438552.6:c.-74A= ENSP00000412566.2:n.-74A=
ENST00000461548.1:c.305-3006A= ENSP00000456213.1:n.305-3006A=
NM_003091.3:c.-74A= NP_003082.1:n.-74A=
NM_198216.1:c.-74A= NP_937859.1:n.-74A=
NM_003091.4:c.-74A= MANE Select NP_003082.1:n.-74A=
NM_198216.2:c.-74A= NP_937859.1:n.-74A=