Canonical Allele Identifier: CA6058143

Gene: SNHG1

Linked Data

• dbSNP Id: rs774287559
• ExAC: 11:62622558 T / TCA
• gnomAD v2: 11-62622558-T-TCA
• gnomAD v3: 11-62855086-T-TCA
• gnomAD v4: 11-62855086-T-TCA
• MyVariant Identifiers: chr11:g.62622558_62622559insCA (hg19) ; chr11:g.62855086_62855087insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855086_62855087insCA , CM000673.2:g.62855086_62855087insCA	GRCh38
NC_000011.9:g.62622558_62622559insCA , CM000673.1:g.62622558_62622559insCA	GRCh37
NC_000011.8:g.62379134_62379135insCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.151+46_151+47insTG
NR_003098.2:n.148+46_148+47insTG
NR_152575.1:n.546+46_546+47insTG
NR_152576.1:n.538+46_538+47insTG
NR_152577.1:n.148+46_148+47insTG
NR_152578.1:n.105+46_105+47insTG
NR_152579.1:n.148+46_148+47insTG
NR_152580.1:n.148+46_148+47insTG
NR_152581.1:n.148+46_148+47insTG
NR_152582.1:n.105+46_105+47insTG
NR_152583.1:n.148+46_148+47insTG
NR_152584.1:n.546+46_546+47insTG
NR_152585.1:n.546+46_546+47insTG