Canonical Allele Identifier: CA9174530
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs372199759
ExAC: 19:9237114 G / A
gnomAD v2: 19-9237114-G-A
gnomAD v3: 19-9126438-G-A
gnomAD v4: 19-9126438-G-A
MyVariant Identifiers: chr19:g.9237114G>A (hg19) chr19:g.9126438G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126438G>A , CM000681.2:g.9126438G>A GRCh38
NC_000019.9:g.9237114G>A , CM000681.1:g.9237114G>A GRCh37
NC_000019.8:g.9098114G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.513C>T MANE Select ENSP00000302867.2:p.Asp171=
NM_001001958.1:c.513C>T MANE Select NP_001001958.1:p.Asp171=
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