Canonical Allele Identifier: CA403789296

Gene: OR7G3

Linked Data

• dbSNP Id: rs1245057849
• gnomAD v2: 19-9237368-C-T
• gnomAD v4: 19-9126692-C-T
• MyVariant Identifiers: chr19:g.9237368C>T (hg19) ; chr19:g.9126692C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126692C>T , CM000681.2:g.9126692C>T	GRCh38
NC_000019.9:g.9237368C>T , CM000681.1:g.9237368C>T	GRCh37
NC_000019.8:g.9098368C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.259G>A MANE Select	ENSP00000302867.2:p.Ala87Thr
NM_001001958.1:c.259G>A MANE Select	NP_001001958.1:p.Ala87Thr