Canonical Allele Identifier: CA403788818

Gene: OR7G3

Linked Data

• dbSNP Id: rs1436639409
• gnomAD v2: 19-9237316-A-G
• gnomAD v4: 19-9126640-A-G
• MyVariant Identifiers: chr19:g.9237316A>G (hg19) ; chr19:g.9126640A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126640A>G , CM000681.2:g.9126640A>G	GRCh38
NC_000019.9:g.9237316A>G , CM000681.1:g.9237316A>G	GRCh37
NC_000019.8:g.9098316A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.311T>C MANE Select	ENSP00000302867.2:p.Val104Ala
NM_001001958.1:c.311T>C MANE Select	NP_001001958.1:p.Val104Ala