Canonical Allele Identifier: CA403788185
Gene: OR7G3 HGNC NCBI

Linked Data

gnomAD v4: 19-9126553-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126553T>A , CM000681.2:g.9126553T>A GRCh38
NC_000019.9:g.9237229T>A , CM000681.1:g.9237229T>A GRCh37
NC_000019.8:g.9098229T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.398A>T MANE Select ENSP00000302867.2:p.Asn133Ile
NM_001001958.1:c.398A>T MANE Select NP_001001958.1:p.Asn133Ile