Canonical Allele Identifier: CA6058209

Gene: SNHG1

Linked Data

• dbSNP Id: rs749587829
• ExAC: 11:62622845 CCA / C
• gnomAD v2: 11-62622845-CCA-C
• gnomAD v3: 11-62855373-CCA-C
• gnomAD v4: 11-62855373-CCA-C
• MyVariant Identifiers: chr11:g.62622846_62622847del (hg19) ; chr11:g.62855374_62855375del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855379_62855380del , CM000673.2:g.62855379_62855380del	GRCh38
NC_000011.9:g.62622851_62622852del , CM000673.1:g.62622851_62622852del	GRCh37
NC_000011.8:g.62379427_62379428del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.67+49_67+50del
NR_003098.2:n.64+49_64+50del
NR_152575.1:n.462+49_462+50del
NR_152576.1:n.462+49_462+50del
NR_152577.1:n.64+49_64+50del
NR_152578.1:n.22-159_22-158del
NR_152579.1:n.64+49_64+50del
NR_152580.1:n.64+49_64+50del
NR_152581.1:n.64+49_64+50del
NR_152582.1:n.22-159_22-158del
NR_152583.1:n.64+49_64+50del
NR_152584.1:n.462+49_462+50del
NR_152585.1:n.462+49_462+50del