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: CA53064883

Gene: LINC01965 HGNC NCBI

Linked Data

dbSNP Id: rs564986211

gnomAD v3: 2-103962022-T-C

gnomAD v4: 2-103962022-T-C

MyVariant Identifiers: chr2:g.104578480T>C (hg19) chr2:g.103962022T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.103962022T>C , CM000664.2:g.103962022T>C	GRCh38
NC_000002.11:g.104578480T>C , CM000664.1:g.104578480T>C	GRCh37
NC_000002.10:g.103944912T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001739621.1:n.178+87577T>C
XR_001739623.1:n.178+87577T>C

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