Canonical Allele Identifier: CA2346122593

Gene: SNRPB

Linked Data

• dbSNP Id: rs779382737
• gnomAD v4: 20-2470733-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2470733C>G , CM000682.2:g.2470733C>G	GRCh38
NC_000020.10:g.2451379C>G , CM000682.1:g.2451379C>G	GRCh37
NC_000020.9:g.2399379C>G	NCBI36
NG_042057.1:g.5121G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688423.1:n.55G>C
ENST00000688775.1:n.55G>C
ENST00000689440.1:n.57G>C
ENST00000690623.1:n.7G>C
ENST00000693393.1:n.57G>C
ENST00000381342.7:c.-43G>C MANE Select	ENSP00000370746.3:n.-43G>C
ENST00000339610.10:c.-43G>C	ENSP00000342305.7:n.-43G>C
ENST00000381342.6:c.-43G>C	ENSP00000370746.2:n.-43G>C
ENST00000438552.6:c.-43G>C	ENSP00000412566.2:n.-43G>C
ENST00000461548.1:c.305-2975G>C	ENSP00000456213.1:n.305-2975G>C
NM_003091.3:c.-43G>C	NP_003082.1:n.-43G>C
NM_198216.1:c.-43G>C	NP_937859.1:n.-43G>C
NM_003091.4:c.-43G>C MANE Select	NP_003082.1:n.-43G>C
NM_198216.2:c.-43G>C	NP_937859.1:n.-43G>C