Canonical Allele Identifier: CA223668018

Gene: SNHG1

Linked Data

• dbSNP Id: rs138362598
• MyVariant Identifiers: chr11:g.62622967G>T (hg19) ; chr11:g.62855495G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855495G>T , CM000673.2:g.62855495G>T	GRCh38
NC_000011.9:g.62622967G>T , CM000673.1:g.62622967G>T	GRCh37
NC_000011.8:g.62379543G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.25-29C>A
NR_003098.2:n.22-29C>A
NR_152575.1:n.391C>A
NR_152576.1:n.391C>A
NR_152577.1:n.22-29C>A
NR_152578.1:n.22-279C>A
NR_152579.1:n.22-29C>A
NR_152580.1:n.22-29C>A
NR_152581.1:n.22-29C>A
NR_152582.1:n.22-279C>A
NR_152583.1:n.22-29C>A
NR_152584.1:n.391C>A
NR_152585.1:n.391C>A