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: CA707238792

Gene: LINC01500 HGNC NCBI

Linked Data

dbSNP Id: rs405460

gnomAD v3: 14-58899597-G-A

gnomAD v4: 14-58899597-G-A

MyVariant Identifiers: chr14:g.59366315G>A (hg19) chr14:g.58899597G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.58899597G>A , CM000676.2:g.58899597G>A	GRCh38
NC_000014.8:g.59366315G>A , CM000676.1:g.59366315G>A	GRCh37
NC_000014.7:g.58436068G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_110547.1:n.457+5266G>A

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