Canonical Allele Identifier: CA6058284

Gene: SNHG1

Linked Data

• dbSNP Id: rs746884995
• ExAC: 11:62623108 G / GA
• gnomAD v2: 11-62623108-G-GA
• gnomAD v3: 11-62855636-G-GA
• gnomAD v4: 11-62855636-G-GA
• MyVariant Identifiers: chr11:g.62623108_62623109insA (hg19) ; chr11:g.62855636_62855637insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855637dup , CM000673.2:g.62855637dup	GRCh38
NC_000011.9:g.62623109dup , CM000673.1:g.62623109dup	GRCh37
NC_000011.8:g.62379685dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.25-171dup
NR_003098.2:n.22-171dup
NR_152575.1:n.249dup
NR_152576.1:n.249dup
NR_152577.1:n.22-171dup
NR_152578.1:n.21+228dup
NR_152579.1:n.22-171dup
NR_152580.1:n.22-171dup
NR_152581.1:n.22-171dup
NR_152582.1:n.21+228dup
NR_152583.1:n.22-171dup
NR_152584.1:n.249dup
NR_152585.1:n.249dup