Canonical Allele Identifier: CA403789008
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs751858999
gnomAD v4: 19-9126664-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126664C>A , CM000681.2:g.9126664C>A GRCh38
NC_000019.9:g.9237340C>A , CM000681.1:g.9237340C>A GRCh37
NC_000019.8:g.9098340C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.287G>T MANE Select ENSP00000302867.2:p.Gly96Val
NM_001001958.1:c.287G>T MANE Select NP_001001958.1:p.Gly96Val