Canonical Allele Identifier: CA6058175
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs746208303
ExAC: 11:62622751 C / A
gnomAD v2: 11-62622751-C-A
gnomAD v4: 11-62855279-C-A
MyVariant Identifiers: chr11:g.62622751C>A (hg19) chr11:g.62622751_62622756delinsAGTACA (hg19) chr11:g.62855279C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855279C>A , CM000673.2:g.62855279C>A GRCh38
NC_000011.9:g.62622751C>A , CM000673.1:g.62622751C>A GRCh37
NC_000011.8:g.62379327C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.68-63G>T
NR_003098.2:n.65-63G>T
NR_152575.1:n.463-63G>T
NR_152576.1:n.463-71G>T
NR_152577.1:n.65-63G>T
NR_152578.1:n.22-63G>T
NR_152579.1:n.65-63G>T
NR_152580.1:n.65-63G>T
NR_152581.1:n.65-63G>T
NR_152582.1:n.22-63G>T
NR_152583.1:n.65-63G>T
NR_152584.1:n.463-63G>T
NR_152585.1:n.463-63G>T
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