Canonical Allele Identifier: CA2321775012
Gene: OR7G3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126452T= , CM000681.2:g.9126452T= GRCh38
NC_000019.9:g.9237128T= , CM000681.1:g.9237128T= GRCh37
NC_000019.8:g.9098128T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.499A= MANE Select ENSP00000302867.2:p.Thr167=
NM_001001958.1:c.499A= MANE Select NP_001001958.1:p.Thr167=