Canonical Allele Identifier: CA403789281

Gene: OR7G3

Linked Data

• dbSNP Id: rs1245057849
• MyVariant Identifiers: chr19:g.9237368C>A (hg19) ; chr19:g.9126692C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.259G>T MANE Select	ENSP00000302867.2:p.Ala87Ser
NM_001001958.1:c.259G>T MANE Select	NP_001001958.1:p.Ala87Ser