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: CA589468111

Gene: MIRLET7A1HG HGNC NCBI

Linked Data

dbSNP Id: rs10739971

gnomAD v2: 9-96937680-G-C

gnomAD v3: 9-94175398-G-C

gnomAD v4: 9-94175398-G-C

MyVariant Identifiers: chr9:g.96937680G>C (hg19) chr9:g.94175398G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94175398G>C , CM000671.2:g.94175398G>C	GRCh38
NC_000009.11:g.96937680G>C , CM000671.1:g.96937680G>C	GRCh37
NC_000009.10:g.95977501G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_170274.1:n.125-467G>C
NR_170275.1:n.124+9017G>C
NR_170276.1:n.125-467G>C
NR_170277.1:n.125-7865G>C
NR_170278.1:n.125-467G>C

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