Canonical Allele Identifier: CA223667695
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1004821910
gnomAD v2: 11-62622739-T-G
gnomAD v3: 11-62855267-T-G
gnomAD v4: 11-62855267-T-G
MyVariant Identifiers: chr11:g.62622739T>G (hg19) chr11:g.62855267T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855267T>G , CM000673.2:g.62855267T>G GRCh38
NC_000011.9:g.62622739T>G , CM000673.1:g.62622739T>G GRCh37
NC_000011.8:g.62379315T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.68-51A>C
NR_003098.2:n.65-51A>C
NR_152575.1:n.463-51A>C
NR_152576.1:n.463-59A>C
NR_152577.1:n.65-51A>C
NR_152578.1:n.22-51A>C
NR_152579.1:n.65-51A>C
NR_152580.1:n.65-51A>C
NR_152581.1:n.65-51A>C
NR_152582.1:n.22-51A>C
NR_152583.1:n.65-51A>C
NR_152584.1:n.463-51A>C
NR_152585.1:n.463-51A>C
Search 100 bp 5'
Search 100 bp 3'