Canonical Allele Identifier: CA6058137

Gene: SNHG1

Linked Data

• dbSNP Id: rs768785710
• ExAC: 11:62622539 TGTGTTCATCATGGAGTGGTTA / T
• gnomAD v2: 11-62622539-TGTGTTCATCATGGAGTGGTTA-T
• gnomAD v4: 11-62855067-TGTGTTCATCATGGAGTGGTTA-T
• MyVariant Identifiers: chr11:g.62622540_62622560del (hg19) ; chr11:g.62855068_62855088del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855068_62855088del , CM000673.2:g.62855068_62855088del	GRCh38
NC_000011.9:g.62622540_62622560del , CM000673.1:g.62622540_62622560del	GRCh37
NC_000011.8:g.62379116_62379136del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.151+45_151+65del
NR_003098.2:n.148+45_148+65del
NR_152575.1:n.546+45_546+65del
NR_152576.1:n.538+45_538+65del
NR_152577.1:n.148+45_148+65del
NR_152578.1:n.105+45_105+65del
NR_152579.1:n.148+45_148+65del
NR_152580.1:n.148+45_148+65del
NR_152581.1:n.148+45_148+65del
NR_152582.1:n.105+45_105+65del
NR_152583.1:n.148+45_148+65del
NR_152584.1:n.546+45_546+65del
NR_152585.1:n.546+45_546+65del