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: CA185874422

Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1028964660

gnomAD v3: 8-128531621-G-T

gnomAD v4: 8-128531621-G-T

MyVariant Identifiers: chr8:g.129543867G>T (hg19) chr8:g.128531621G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128531621G>T , CM000670.2:g.128531621G>T	GRCh38
NC_000008.10:g.129543867G>T , CM000670.1:g.129543867G>T	GRCh37
NC_000008.9:g.129613049G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+29449C>A

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