Canonical Allele Identifier: CA1977986501
Gene: SNHG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855780T= , CM000673.2:g.62855780T= GRCh38
NC_000011.9:g.62623252T= , CM000673.1:g.62623252T= GRCh37
NC_000011.8:g.62379828T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.24+85A=
NR_003098.2:n.21+85A=
NR_152575.1:n.106A=
NR_152576.1:n.106A=
NR_152577.1:n.21+85A=
NR_152578.1:n.21+85A=
NR_152579.1:n.21+85A=
NR_152580.1:n.21+85A=
NR_152581.1:n.21+85A=
NR_152582.1:n.21+85A=
NR_152583.1:n.21+85A=
NR_152584.1:n.106A=
NR_152585.1:n.106A=