Canonical Allele Identifier: CA403789568

Gene: OR7G3

Linked Data

• dbSNP Id: rs1347667788
• gnomAD v2: 19-9237395-T-C
• gnomAD v4: 19-9126719-T-C
• MyVariant Identifiers: chr19:g.9237395T>C (hg19) ; chr19:g.9126719T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126719T>C , CM000681.2:g.9126719T>C	GRCh38
NC_000019.9:g.9237395T>C , CM000681.1:g.9237395T>C	GRCh37
NC_000019.8:g.9098395T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.232A>G MANE Select	ENSP00000302867.2:p.Met78Val
NM_001001958.1:c.232A>G MANE Select	NP_001001958.1:p.Met78Val