Canonical Allele Identifier: CA474890218

Gene: SNHG1

Linked Data

• dbSNP Id: rs770582058
• gnomAD v2: 11-62622997-T-G
• gnomAD v3: 11-62855525-T-G
• gnomAD v4: 11-62855525-T-G
• MyVariant Identifiers: chr11:g.62622997T>G (hg19) ; chr11:g.62855525T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855525T>G , CM000673.2:g.62855525T>G	GRCh38
NC_000011.9:g.62622997T>G , CM000673.1:g.62622997T>G	GRCh37
NC_000011.8:g.62379573T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.25-59A>C
NR_003098.2:n.22-59A>C
NR_152575.1:n.361A>C
NR_152576.1:n.361A>C
NR_152577.1:n.22-59A>C
NR_152578.1:n.22-309A>C
NR_152579.1:n.22-59A>C
NR_152580.1:n.22-59A>C
NR_152581.1:n.22-59A>C
NR_152582.1:n.22-309A>C
NR_152583.1:n.22-59A>C
NR_152584.1:n.361A>C
NR_152585.1:n.361A>C