Canonical Allele Identifier: CA403786756
Gene: OR7G3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9237038T>A (hg19) chr19:g.9126362T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126362T>A , CM000681.2:g.9126362T>A GRCh38
NC_000019.9:g.9237038T>A , CM000681.1:g.9237038T>A GRCh37
NC_000019.8:g.9098038T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.589A>T MANE Select ENSP00000302867.2:p.Ile197Phe
NM_001001958.1:c.589A>T MANE Select NP_001001958.1:p.Ile197Phe
Search 100 bp 5'
Search 100 bp 3'