Canonical Allele Identifier: CA474889260
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1289045771

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855170G>A , CM000673.2:g.62855170G>A GRCh38
NC_000011.9:g.62622642G>A , CM000673.1:g.62622642G>A GRCh37
NC_000011.8:g.62379218G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.114C>T
NR_003098.2:n.111C>T
NR_152575.1:n.509C>T
NR_152576.1:n.501C>T
NR_152577.1:n.111C>T
NR_152578.1:n.68C>T
NR_152579.1:n.111C>T
NR_152580.1:n.111C>T
NR_152581.1:n.111C>T
NR_152582.1:n.68C>T
NR_152583.1:n.111C>T
NR_152584.1:n.509C>T
NR_152585.1:n.509C>T