Canonical Allele Identifier: CA6058174

Gene: SNHG1

Linked Data

• dbSNP Id: rs764860453
• ExAC: 11:62622751 CGTACA / C
• gnomAD v2: 11-62622751-CGTACA-C
• gnomAD v3: 11-62855279-CGTACA-C
• gnomAD v4: 11-62855279-CGTACA-C
• MyVariant Identifiers: chr11:g.62622752_62622756del (hg19) ; chr11:g.62855280_62855284del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855287_62855291del , CM000673.2:g.62855287_62855291del	GRCh38
NC_000011.9:g.62622759_62622763del , CM000673.1:g.62622759_62622763del	GRCh37
NC_000011.8:g.62379335_62379339del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.68-68_68-64del
NR_003098.2:n.65-68_65-64del
NR_152575.1:n.463-68_463-64del
NR_152576.1:n.463-76_463-72del
NR_152577.1:n.65-68_65-64del
NR_152578.1:n.22-68_22-64del
NR_152579.1:n.65-68_65-64del
NR_152580.1:n.65-68_65-64del
NR_152581.1:n.65-68_65-64del
NR_152582.1:n.22-68_22-64del
NR_152583.1:n.65-68_65-64del
NR_152584.1:n.463-68_463-64del
NR_152585.1:n.463-68_463-64del