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: CA185874419

Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs963664524

gnomAD v3: 8-128531606-T-C

gnomAD v4: 8-128531606-T-C

MyVariant Identifiers: chr8:g.129543852T>C (hg19) chr8:g.128531606T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128531606T>C , CM000670.2:g.128531606T>C	GRCh38
NC_000008.10:g.129543852T>C , CM000670.1:g.129543852T>C	GRCh37
NC_000008.9:g.129613034T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+29464A>G

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