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: CA403790164

Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1338374137

gnomAD v3: 19-9126775-A-C

gnomAD v4: 19-9126775-A-C

MyVariant Identifiers: chr19:g.9237451A>C (hg19) chr19:g.9126775A>C (hg38)

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Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126775A>C , CM000681.2:g.9126775A>C	GRCh38
NC_000019.9:g.9237451A>C , CM000681.1:g.9237451A>C	GRCh37
NC_000019.8:g.9098451A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000305444.2:c.176T>G MANE Select	ENSP00000302867.2:p.Met59Arg
NM_001001958.1:c.176T>G MANE Select	NP_001001958.1:p.Met59Arg

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