Canonical Allele Identifier: CA2321775162
Gene: OR7G3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126779G= , CM000681.2:g.9126779G= GRCh38
NC_000019.9:g.9237455G= , CM000681.1:g.9237455G= GRCh37
NC_000019.8:g.9098455G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305444.2:c.172C= MANE Select ENSP00000302867.2:p.Pro58=
NM_001001958.1:c.172C= MANE Select NP_001001958.1:p.Pro58=