Canonical Allele Identifier: CA403787179
Gene: OR7G3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3206679
ClinVar RCV Id: RCV004502062
dbSNP Id: rs2050509604
MyVariant Identifiers: chr19:g.9237085A>G (hg19) chr19:g.9126409A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126409A>G , CM000681.2:g.9126409A>G GRCh38
NC_000019.9:g.9237085A>G , CM000681.1:g.9237085A>G GRCh37
NC_000019.8:g.9098085A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.542T>C MANE Select ENSP00000302867.2:p.Leu181Pro
NM_001001958.1:c.542T>C MANE Select NP_001001958.1:p.Leu181Pro
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