Canonical Allele Identifier: CA6058159

Gene: SNHG1

Linked Data

• dbSNP Id: rs750029109
• ExAC: 11:62622599 A / G
• gnomAD v2: 11-62622599-A-G
• gnomAD v3: 11-62855127-A-G
• gnomAD v4: 11-62855127-A-G
• MyVariant Identifiers: chr11:g.62622599A>G (hg19) ; chr11:g.62855127A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855127A>G , CM000673.2:g.62855127A>G	GRCh38
NC_000011.9:g.62622599A>G , CM000673.1:g.62622599A>G	GRCh37
NC_000011.8:g.62379175A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.151+6T>C
NR_003098.2:n.148+6T>C
NR_152575.1:n.546+6T>C
NR_152576.1:n.538+6T>C
NR_152577.1:n.148+6T>C
NR_152578.1:n.105+6T>C
NR_152579.1:n.148+6T>C
NR_152580.1:n.148+6T>C
NR_152581.1:n.148+6T>C
NR_152582.1:n.105+6T>C
NR_152583.1:n.148+6T>C
NR_152584.1:n.546+6T>C
NR_152585.1:n.546+6T>C