Canonical Allele Identifier: CA6058297
Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs532041289
ExAC: 11:62623144 C / T
gnomAD v2: 11-62623144-C-T
gnomAD v3: 11-62855672-C-T
gnomAD v4: 11-62855672-C-T
MyVariant Identifiers: chr11:g.62623144C>T (hg19) chr11:g.62855672C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62855672C>T , CM000673.2:g.62855672C>T GRCh38
NC_000011.9:g.62623144C>T , CM000673.1:g.62623144C>T GRCh37
NC_000011.8:g.62379720C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_003098.1:n.24+193G>A
NR_003098.2:n.21+193G>A
NR_152575.1:n.214G>A
NR_152576.1:n.214G>A
NR_152577.1:n.21+193G>A
NR_152578.1:n.21+193G>A
NR_152579.1:n.21+193G>A
NR_152580.1:n.21+193G>A
NR_152581.1:n.21+193G>A
NR_152582.1:n.21+193G>A
NR_152583.1:n.21+193G>A
NR_152584.1:n.214G>A
NR_152585.1:n.214G>A
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