Canonical Allele Identifier: CA474890128
Gene: SNHG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.62622961A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855489A>T , CM000673.2:g.62855489A>T GRCh38
NC_000011.9:g.62622961A>T , CM000673.1:g.62622961A>T GRCh37
NC_000011.8:g.62379537A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_003098.1:n.25-23T>A
NR_003098.2:n.22-23T>A
NR_152575.1:n.397T>A
NR_152576.1:n.397T>A
NR_152577.1:n.22-23T>A
NR_152578.1:n.22-273T>A
NR_152579.1:n.22-23T>A
NR_152580.1:n.22-23T>A
NR_152581.1:n.22-23T>A
NR_152582.1:n.22-273T>A
NR_152583.1:n.22-23T>A
NR_152584.1:n.397T>A
NR_152585.1:n.397T>A