Canonical Allele Identifier: CA1977986190
Gene: SNHG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855655C= , CM000673.2:g.62855655C= GRCh38
NC_000011.9:g.62623127C= , CM000673.1:g.62623127C= GRCh37
NC_000011.8:g.62379703C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.25-189G=
NR_003098.2:n.22-189G=
NR_152575.1:n.231G=
NR_152576.1:n.231G=
NR_152577.1:n.22-189G=
NR_152578.1:n.21+210G=
NR_152579.1:n.22-189G=
NR_152580.1:n.22-189G=
NR_152581.1:n.22-189G=
NR_152582.1:n.21+210G=
NR_152583.1:n.22-189G=
NR_152584.1:n.231G=
NR_152585.1:n.231G=