Canonical Allele Identifier: CA6058216

Gene: SNHG1

Linked Data

• dbSNP Id: rs752533492
• ExAC: 11:62622867 G / A
• gnomAD v2: 11-62622867-G-A
• gnomAD v3: 11-62855395-G-A
• gnomAD v4: 11-62855395-G-A
• MyVariant Identifiers: chr11:g.62622867G>A (hg19) ; chr11:g.62855395G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855395G>A , CM000673.2:g.62855395G>A	GRCh38
NC_000011.9:g.62622867G>A , CM000673.1:g.62622867G>A	GRCh37
NC_000011.8:g.62379443G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.67+29C>T
NR_003098.2:n.64+29C>T
NR_152575.1:n.462+29C>T
NR_152576.1:n.462+29C>T
NR_152577.1:n.64+29C>T
NR_152578.1:n.22-179C>T
NR_152579.1:n.64+29C>T
NR_152580.1:n.64+29C>T
NR_152581.1:n.64+29C>T
NR_152582.1:n.22-179C>T
NR_152583.1:n.64+29C>T
NR_152584.1:n.462+29C>T
NR_152585.1:n.462+29C>T