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: CA53064888

Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs772639383

gnomAD v3: 2-103962038-G-A

gnomAD v4: 2-103962038-G-A

MyVariant Identifiers: chr2:g.104578496G>A (hg19) chr2:g.103962038G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962038G>A , CM000664.2:g.103962038G>A	GRCh38
NC_000002.11:g.104578496G>A , CM000664.1:g.104578496G>A	GRCh37
NC_000002.10:g.103944928G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001739621.1:n.178+87593G>A
XR_001739623.1:n.178+87593G>A

Search 100 bp 5'

Search 100 bp 3'