Canonical Allele Identifier: CA474889970

Gene: SNHG1

Linked Data

• dbSNP Id: rs1480203848
• MyVariant Identifiers: chr11:g.62622904C>T (hg19) ; chr11:g.62855432C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855432C>T , CM000673.2:g.62855432C>T	GRCh38
NC_000011.9:g.62622904C>T , CM000673.1:g.62622904C>T	GRCh37
NC_000011.8:g.62379480C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.59G>A
NR_003098.2:n.56G>A
NR_152575.1:n.454G>A
NR_152576.1:n.454G>A
NR_152577.1:n.56G>A
NR_152578.1:n.22-216G>A
NR_152579.1:n.56G>A
NR_152580.1:n.56G>A
NR_152581.1:n.56G>A
NR_152582.1:n.22-216G>A
NR_152583.1:n.56G>A
NR_152584.1:n.454G>A
NR_152585.1:n.454G>A