Canonical Allele Identifier: CA2321775158
Gene: OR7G3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126775A= , CM000681.2:g.9126775A= GRCh38
NC_000019.9:g.9237451A= , CM000681.1:g.9237451A= GRCh37
NC_000019.8:g.9098451A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305444.2:c.176T= MANE Select ENSP00000302867.2:p.Met59=
NM_001001958.1:c.176T= MANE Select NP_001001958.1:p.Met59=