Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

Canonical Allele Identifier: CA474890116

Gene: SNHG1 HGNC NCBI

Linked Data

dbSNP Id: rs879223875

MyVariant Identifiers: chr11:g.62622957T>G (hg19) chr11:g.62855485T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62855485T>G , CM000673.2:g.62855485T>G	GRCh38
NC_000011.9:g.62622957T>G , CM000673.1:g.62622957T>G	GRCh37
NC_000011.8:g.62379533T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_003098.1:n.25-19A>C
NR_003098.2:n.22-19A>C
NR_152575.1:n.401A>C
NR_152576.1:n.401A>C
NR_152577.1:n.22-19A>C
NR_152578.1:n.22-269A>C
NR_152579.1:n.22-19A>C
NR_152580.1:n.22-19A>C
NR_152581.1:n.22-19A>C
NR_152582.1:n.22-269A>C
NR_152583.1:n.22-19A>C
NR_152584.1:n.401A>C
NR_152585.1:n.401A>C

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