Canonical Allele Identifier: CA6058155

Gene: SNHG1

Linked Data

• dbSNP Id: rs760488244
• ExAC: 11:62622587 T / TA
• gnomAD v2: 11-62622587-T-TA
• gnomAD v3: 11-62855115-T-TA
• gnomAD v4: 11-62855115-T-TA
• MyVariant Identifiers: chr11:g.62622587_62622588insA (hg19) ; chr11:g.62855115_62855116insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855118dup , CM000673.2:g.62855118dup	GRCh38
NC_000011.9:g.62622590dup , CM000673.1:g.62622590dup	GRCh37
NC_000011.8:g.62379166dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.151+17dup
NR_003098.2:n.148+17dup
NR_152575.1:n.546+17dup
NR_152576.1:n.538+17dup
NR_152577.1:n.148+17dup
NR_152578.1:n.105+17dup
NR_152579.1:n.148+17dup
NR_152580.1:n.148+17dup
NR_152581.1:n.148+17dup
NR_152582.1:n.105+17dup
NR_152583.1:n.148+17dup
NR_152584.1:n.546+17dup
NR_152585.1:n.546+17dup