Canonical Allele Identifier: CA2346122664
Gene: SNRPB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470804T= , CM000682.2:g.2470804T= GRCh38
NC_000020.10:g.2451450T= , CM000682.1:g.2451450T= GRCh37
NC_000020.9:g.2399450T= NCBI36
NG_042057.1:g.5050A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339610.10:c.-114A= ENSP00000342305.7:n.-114A=
ENST00000381342.6:c.-114A= ENSP00000370746.2:n.-114A=
ENST00000438552.6:c.-114A= ENSP00000412566.2:n.-114A=
ENST00000461548.1:c.305-3046A= ENSP00000456213.1:n.305-3046A=
NM_003091.3:c.-114A= NP_003082.1:n.-114A=
NM_198216.1:c.-114A= NP_937859.1:n.-114A=
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