Canonical Allele Identifier: CA310850148
Gene: SNRPB HGNC NCBI

Linked Data

dbSNP Id: rs1030914511
gnomAD v3: 20-2470849-G-C
gnomAD v4: 20-2470849-G-C
MyVariant Identifiers: chr20:g.2451495G>C (hg19) chr20:g.2470849G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2470849G>C , CM000682.2:g.2470849G>C GRCh38
NC_000020.10:g.2451495G>C , CM000682.1:g.2451495G>C GRCh37
NC_000020.9:g.2399495G>C NCBI36
NG_042057.1:g.5005C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381342.6:c.-159C>G ENSP00000370746.2:n.-159C>G
ENST00000438552.6:c.-159C>G ENSP00000412566.2:n.-159C>G
ENST00000461548.1:c.305-3091C>G ENSP00000456213.1:n.305-3091C>G
NM_003091.3:c.-159C>G NP_003082.1:n.-159C>G
NM_198216.1:c.-159C>G NP_937859.1:n.-159C>G
Search 100 bp 5'
Search 100 bp 3'