Canonical Allele Identifier: CA1977986216
Gene: SNHG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855662T= , CM000673.2:g.62855662T= GRCh38
NC_000011.9:g.62623134T= , CM000673.1:g.62623134T= GRCh37
NC_000011.8:g.62379710T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.25-196A=
NR_003098.2:n.22-196A=
NR_152575.1:n.224A=
NR_152576.1:n.224A=
NR_152577.1:n.22-196A=
NR_152578.1:n.21+203A=
NR_152579.1:n.22-196A=
NR_152580.1:n.22-196A=
NR_152581.1:n.22-196A=
NR_152582.1:n.21+203A=
NR_152583.1:n.22-196A=
NR_152584.1:n.224A=
NR_152585.1:n.224A=
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