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: CA137022020

Gene: HLA-DQA1 HGNC NCBI

Linked Data

dbSNP Id: rs17612900

gnomAD v2: 6-32620838-G-C

gnomAD v3: 6-32653061-G-C

gnomAD v4: 6-32653061-G-C

MyVariant Identifiers: chr6:g.32620838G>C (hg19) chr6:g.32653061G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32653061G>C , CM000668.2:g.32653061G>C	GRCh38
NC_000006.11:g.32620838G>C , CM000668.1:g.32620838G>C	GRCh37
NC_000006.10:g.32728816G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_006715079.2:c.614-1606G>C	XP_006715142.1:n.614-1606G>C
XM_006715079.4:c.614-1606G>C	XP_006715142.1:n.614-1606G>C

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