Canonical Allele Identifier: CA9174532
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs779971052
ExAC: 19:9237126 G / A
gnomAD v2: 19-9237126-G-A
gnomAD v4: 19-9126450-G-A
MyVariant Identifiers: chr19:g.9237126G>A (hg19) chr19:g.9126450G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126450G>A , CM000681.2:g.9126450G>A GRCh38
NC_000019.9:g.9237126G>A , CM000681.1:g.9237126G>A GRCh37
NC_000019.8:g.9098126G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.501C>T MANE Select ENSP00000302867.2:p.Thr167=
NM_001001958.1:c.501C>T MANE Select NP_001001958.1:p.Thr167=
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