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: CA197961796

Gene: LINC01492 HGNC NCBI

Linked Data

dbSNP Id: rs893584721

gnomAD v3: 9-103261897-G-A

gnomAD v4: 9-103261897-G-A

MyVariant Identifiers: chr9:g.106024179G>A (hg19) chr9:g.103261897G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.103261897G>A , CM000671.2:g.103261897G>A	GRCh38
NC_000009.11:g.106024179G>A , CM000671.1:g.106024179G>A	GRCh37
NC_000009.10:g.105064000G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121578.1:n.771+2627C>T

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