Canonical Allele Identifier: CA403788943

Gene: OR7G3

Linked Data

• ClinVar Variation Id: 2458914
• ClinVar RCV Id: RCV004250952
• dbSNP Id: rs2050511811
• gnomAD v4: 19-9126656-T-A
• MyVariant Identifiers: chr19:g.9237332T>A (hg19) ; chr19:g.9126656T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.295A>T MANE Select	ENSP00000302867.2:p.Thr99Ser
NM_001001958.1:c.295A>T MANE Select	NP_001001958.1:p.Thr99Ser