Canonical Allele Identifier: CA474890539
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs1351241129

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855654T>G , CM000673.2:g.62855654T>G GRCh38
NC_000011.9:g.62623126T>G , CM000673.1:g.62623126T>G GRCh37
NC_000011.8:g.62379702T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.25-188A>C
NR_003098.2:n.22-188A>C
NR_152575.1:n.232A>C
NR_152576.1:n.232A>C
NR_152577.1:n.22-188A>C
NR_152578.1:n.21+211A>C
NR_152579.1:n.22-188A>C
NR_152580.1:n.22-188A>C
NR_152581.1:n.22-188A>C
NR_152582.1:n.21+211A>C
NR_152583.1:n.22-188A>C
NR_152584.1:n.232A>C
NR_152585.1:n.232A>C