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: CA403791251

Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs2050514203

gnomAD v3: 19-9126874-A-G

gnomAD v4: 19-9126874-A-G

MyVariant Identifiers: chr19:g.9237550A>G (hg19) chr19:g.9126874A>G (hg38)

JSON-LD

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126874A>G , CM000681.2:g.9126874A>G	GRCh38
NC_000019.9:g.9237550A>G , CM000681.1:g.9237550A>G	GRCh37
NC_000019.8:g.9098550A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000305444.2:c.77T>C MANE Select	ENSP00000302867.2:p.Ile26Thr
NM_001001958.1:c.77T>C MANE Select	NP_001001958.1:p.Ile26Thr

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