Canonical Allele Identifier: CA2321774998
Gene: OR7G3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126420A= , CM000681.2:g.9126420A= GRCh38
NC_000019.9:g.9237096A= , CM000681.1:g.9237096A= GRCh37
NC_000019.8:g.9098096A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.531T= MANE Select ENSP00000302867.2:p.Phe177=
NM_001001958.1:c.531T= MANE Select NP_001001958.1:p.Phe177=