Canonical Allele Identifier: CA223667600
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs945676811
gnomAD v3: 11-62855110-G-A
gnomAD v4: 11-62855110-G-A
MyVariant Identifiers: chr11:g.62622582G>A (hg19) chr11:g.62855110G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855110G>A , CM000673.2:g.62855110G>A GRCh38
NC_000011.9:g.62622582G>A , CM000673.1:g.62622582G>A GRCh37
NC_000011.8:g.62379158G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.151+23C>T
NR_003098.2:n.148+23C>T
NR_152575.1:n.546+23C>T
NR_152576.1:n.538+23C>T
NR_152577.1:n.148+23C>T
NR_152578.1:n.105+23C>T
NR_152579.1:n.148+23C>T
NR_152580.1:n.148+23C>T
NR_152581.1:n.148+23C>T
NR_152582.1:n.105+23C>T
NR_152583.1:n.148+23C>T
NR_152584.1:n.546+23C>T
NR_152585.1:n.546+23C>T
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