Canonical Allele Identifier: CA474890226

Gene: SNHG1

Linked Data

• dbSNP Id: rs1463396334
• gnomAD v2: 11-62623000-C-G
• gnomAD v4: 11-62855528-C-G
• MyVariant Identifiers: chr11:g.62623000C>G (hg19) ; chr11:g.62855528C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855528C>G , CM000673.2:g.62855528C>G	GRCh38
NC_000011.9:g.62623000C>G , CM000673.1:g.62623000C>G	GRCh37
NC_000011.8:g.62379576C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.25-62G>C
NR_003098.2:n.22-62G>C
NR_152575.1:n.358G>C
NR_152576.1:n.358G>C
NR_152577.1:n.22-62G>C
NR_152578.1:n.22-312G>C
NR_152579.1:n.22-62G>C
NR_152580.1:n.22-62G>C
NR_152581.1:n.22-62G>C
NR_152582.1:n.22-312G>C
NR_152583.1:n.22-62G>C
NR_152584.1:n.358G>C
NR_152585.1:n.358G>C