Canonical Allele Identifier: CA742353388

Gene: SNRPB

Linked Data

• dbSNP Id: rs1410160673
• gnomAD v3: 20-2470754-C-G
• gnomAD v4: 20-2470754-C-G
• MyVariant Identifiers: chr20:g.2451400C>G (hg19) ; chr20:g.2470754C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.2470754C>G , CM000682.2:g.2470754C>G	GRCh38
NC_000020.10:g.2451400C>G , CM000682.1:g.2451400C>G	GRCh37
NC_000020.9:g.2399400C>G	NCBI36
NG_042057.1:g.5100G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000688423.1:n.34G>C
ENST00000688775.1:n.34G>C
ENST00000689440.1:n.36G>C
ENST00000693393.1:n.36G>C
ENST00000381342.7:c.-64G>C MANE Select	ENSP00000370746.3:n.-64G>C
ENST00000339610.10:c.-64G>C	ENSP00000342305.7:n.-64G>C
ENST00000381342.6:c.-64G>C	ENSP00000370746.2:n.-64G>C
ENST00000438552.6:c.-64G>C	ENSP00000412566.2:n.-64G>C
ENST00000461548.1:c.305-2996G>C	ENSP00000456213.1:n.305-2996G>C
NM_003091.3:c.-64G>C	NP_003082.1:n.-64G>C
NM_198216.1:c.-64G>C	NP_937859.1:n.-64G>C
NM_003091.4:c.-64G>C MANE Select	NP_003082.1:n.-64G>C
NM_198216.2:c.-64G>C	NP_937859.1:n.-64G>C