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: CA669931508

Gene: HECTD2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1477632953

gnomAD v3: 10-91590066-T-C

gnomAD v4: 10-91590066-T-C

MyVariant Identifiers: chr10:g.93349823T>C (hg19) chr10:g.91590066T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.91590066T>C , CM000672.2:g.91590066T>C	GRCh38
NC_000010.10:g.93349823T>C , CM000672.1:g.93349823T>C	GRCh37
NC_000010.9:g.93339803T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_024467.1:n.110+21285A>G

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