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: CA137815787

Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs973812684

gnomAD v3: 6-40353964-T-A

gnomAD v4: 6-40353964-T-A

MyVariant Identifiers: chr6:g.40321703T>A (hg19) chr6:g.40353964T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40353964T>A , CM000668.2:g.40353964T>A	GRCh38
NC_000006.11:g.40321703T>A , CM000668.1:g.40321703T>A	GRCh37
NC_000006.10:g.40429681T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038887.1:n.2043A>T

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