Canonical Allele Identifier: CA403788949

Gene: OR7G3

Linked Data

• MyVariant Identifiers: chr19:g.9237332T>G (hg19) ; chr19:g.9126656T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126656T>G , CM000681.2:g.9126656T>G	GRCh38
NC_000019.9:g.9237332T>G , CM000681.1:g.9237332T>G	GRCh37
NC_000019.8:g.9098332T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.295A>C MANE Select	ENSP00000302867.2:p.Thr99Pro
NM_001001958.1:c.295A>C MANE Select	NP_001001958.1:p.Thr99Pro