Canonical Allele Identifier: CA186110

Gene: SNRPB

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2467305C>G , CM000682.2:g.2467305C>G	GRCh38
NC_000020.10:g.2447951C>G , CM000682.1:g.2447951C>G	GRCh37
NC_000020.9:g.2395951C>G	NCBI36
NG_042057.1:g.8549G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688423.1:n.554G>C
ENST00000688775.1:n.554G>C
ENST00000689440.1:n.265G>C
ENST00000690623.1:n.215G>C
ENST00000693393.1:n.556G>C
ENST00000381342.7:c.155+302G>C MANE Select	ENSP00000370746.3:n.155+302G>C
ENST00000339610.10:c.155+302G>C	ENSP00000342305.7:n.155+302G>C
ENST00000381342.6:c.155+302G>C	ENSP00000370746.2:n.155+302G>C
ENST00000438552.6:c.155+302G>C	ENSP00000412566.2:n.155+302G>C
ENST00000461548.1:c.*125G>C	ENSP00000456213.1:n.*125G>C
ENST00000474384.2:c.166G>C	ENSP00000474579.1:p.Gly56Arg
NM_003091.3:c.155+302G>C	NP_003082.1:n.155+302G>C
NM_198216.1:c.155+302G>C	NP_937859.1:n.155+302G>C
NM_003091.4:c.155+302G>C MANE Select	NP_003082.1:n.155+302G>C
NM_198216.2:c.155+302G>C	NP_937859.1:n.155+302G>C