Canonical Allele Identifier: CA474890136
Gene: SNHG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.62622964T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855492T>C , CM000673.2:g.62855492T>C GRCh38
NC_000011.9:g.62622964T>C , CM000673.1:g.62622964T>C GRCh37
NC_000011.8:g.62379540T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003098.1:n.25-26A>G
NR_003098.2:n.22-26A>G
NR_152575.1:n.394A>G
NR_152576.1:n.394A>G
NR_152577.1:n.22-26A>G
NR_152578.1:n.22-276A>G
NR_152579.1:n.22-26A>G
NR_152580.1:n.22-26A>G
NR_152581.1:n.22-26A>G
NR_152582.1:n.22-276A>G
NR_152583.1:n.22-26A>G
NR_152584.1:n.394A>G
NR_152585.1:n.394A>G