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: CA232144107

Gene: LINC02714 HGNC NCBI

Linked Data

dbSNP Id: rs1039850390

gnomAD v3: 11-134756913-G-A

gnomAD v4: 11-134756913-G-A

MyVariant Identifiers: chr11:g.134626807G>A (hg19) chr11:g.134756913G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134756913G>A , CM000673.2:g.134756913G>A	GRCh38
NC_000011.9:g.134626807G>A , CM000673.1:g.134626807G>A	GRCh37
NC_000011.8:g.134132017G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_147836.1:n.599-4161G>A

Search 100 bp 5'

Search 100 bp 3'