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: CA717519525

Gene: NR2F2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1468052970

gnomAD v3: 15-96287172-G-A

gnomAD v4: 15-96287172-G-A

MyVariant Identifiers: chr15:g.96830401G>A (hg19) chr15:g.96287172G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96287172G>A , CM000677.2:g.96287172G>A	GRCh38
NC_000015.9:g.96830401G>A , CM000677.1:g.96830401G>A	GRCh37
NC_000015.8:g.94631405G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_102743.1:n.409+1492C>T
NR_125738.1:n.317+3458C>T

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