Canonical Allele Identifier: CA310850079
Gene: SNRPB HGNC NCBI

Linked Data

dbSNP Id: rs1046305732
gnomAD v3: 20-2470798-G-C
gnomAD v4: 20-2470798-G-C
MyVariant Identifiers: chr20:g.2451444G>C (hg19) chr20:g.2470798G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470798G>C , CM000682.2:g.2470798G>C GRCh38
NC_000020.10:g.2451444G>C , CM000682.1:g.2451444G>C GRCh37
NC_000020.9:g.2399444G>C NCBI36
NG_042057.1:g.5056C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339610.10:c.-108C>G ENSP00000342305.7:n.-108C>G
ENST00000381342.6:c.-108C>G ENSP00000370746.2:n.-108C>G
ENST00000438552.6:c.-108C>G ENSP00000412566.2:n.-108C>G
ENST00000461548.1:c.305-3040C>G ENSP00000456213.1:n.305-3040C>G
NM_003091.3:c.-108C>G NP_003082.1:n.-108C>G
NM_198216.1:c.-108C>G NP_937859.1:n.-108C>G
Search 100 bp 5'
Search 100 bp 3'