Canonical Allele Identifier: CA599798952

Gene: SNHG1

Linked Data

• dbSNP Id: rs1565236707
• gnomAD v2: 11-62622850-CACTCA-C
• gnomAD v3: 11-62855378-CACTCA-C
• gnomAD v4: 11-62855378-CACTCA-C
• MyVariant Identifiers: chr11:g.62622851_62622855del (hg19) ; chr11:g.62855379_62855383del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855381_62855385del , CM000673.2:g.62855381_62855385del	GRCh38
NC_000011.9:g.62622853_62622857del , CM000673.1:g.62622853_62622857del	GRCh37
NC_000011.8:g.62379429_62379433del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_003098.1:n.67+41_67+45del
NR_003098.2:n.64+41_64+45del
NR_152575.1:n.462+41_462+45del
NR_152576.1:n.462+41_462+45del
NR_152577.1:n.64+41_64+45del
NR_152578.1:n.22-167_22-163del
NR_152579.1:n.64+41_64+45del
NR_152580.1:n.64+41_64+45del
NR_152581.1:n.64+41_64+45del
NR_152582.1:n.22-167_22-163del
NR_152583.1:n.64+41_64+45del
NR_152584.1:n.462+41_462+45del
NR_152585.1:n.462+41_462+45del