Canonical Allele Identifier: CA599798956

Gene: SNHG1

Linked Data

• dbSNP Id: rs1354647982
• gnomAD v2: 11-62623358-A-T
• MyVariant Identifiers: chr11:g.62623358A>T (hg19) ; chr11:g.62855886A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855886A>T , CM000673.2:g.62855886A>T	GRCh38
NC_000011.9:g.62623358A>T , CM000673.1:g.62623358A>T	GRCh37
NC_000011.8:g.62379934A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.3T>A