Canonical Allele Identifier: CA403786401

Gene: OR7G3

Linked Data

• dbSNP Id: rs779628562
• MyVariant Identifiers: chr19:g.9236984T>C (hg19) ; chr19:g.9126308T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126308T>C , CM000681.2:g.9126308T>C	GRCh38
NC_000019.9:g.9236984T>C , CM000681.1:g.9236984T>C	GRCh37
NC_000019.8:g.9097984T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.643A>G MANE Select	ENSP00000302867.2:p.Ile215Val
NM_001001958.1:c.643A>G MANE Select	NP_001001958.1:p.Ile215Val