Canonical Allele Identifier: CA9174496
Gene: OR7G3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2649275
ClinVar RCV Id: RCV003421822
dbSNP Id: rs139482540
ExAC: 19:9236967 T / C
gnomAD v2: 19-9236967-T-C
gnomAD v3: 19-9126291-T-C
gnomAD v4: 19-9126291-T-C
MyVariant Identifiers: chr19:g.9236967T>C (hg19) chr19:g.9126291T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126291T>C , CM000681.2:g.9126291T>C GRCh38
NC_000019.9:g.9236967T>C , CM000681.1:g.9236967T>C GRCh37
NC_000019.8:g.9097967T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.660A>G MANE Select ENSP00000302867.2:p.Arg220=
NM_001001958.1:c.660A>G MANE Select NP_001001958.1:p.Arg220=
Search 100 bp 5'
Search 100 bp 3'