Canonical Allele Identifier: CA474890041
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1357297795
MyVariant Identifiers: chr11:g.62622929C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855457C>T , CM000673.2:g.62855457C>T GRCh38
NC_000011.9:g.62622929C>T , CM000673.1:g.62622929C>T GRCh37
NC_000011.8:g.62379505C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.34G>A
NR_003098.2:n.31G>A
NR_152575.1:n.429G>A
NR_152576.1:n.429G>A
NR_152577.1:n.31G>A
NR_152578.1:n.22-241G>A
NR_152579.1:n.31G>A
NR_152580.1:n.31G>A
NR_152581.1:n.31G>A
NR_152582.1:n.22-241G>A
NR_152583.1:n.31G>A
NR_152584.1:n.429G>A
NR_152585.1:n.429G>A