Canonical Allele Identifier: CA2321774942
Gene: OR7G3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126291T= , CM000681.2:g.9126291T= GRCh38
NC_000019.9:g.9236967T= , CM000681.1:g.9236967T= GRCh37
NC_000019.8:g.9097967T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.660A= MANE Select ENSP00000302867.2:p.Arg220=
NM_001001958.1:c.660A= MANE Select NP_001001958.1:p.Arg220=