Canonical Allele Identifier: CA305052035

Gene: OR7G3

Linked Data

• dbSNP Id: rs914911297
• gnomAD v3: 19-9126865-A-G
• gnomAD v4: 19-9126865-A-G
• MyVariant Identifiers: chr19:g.9237541A>G (hg19) ; chr19:g.9126865A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126865A>G , CM000681.2:g.9126865A>G	GRCh38
NC_000019.9:g.9237541A>G , CM000681.1:g.9237541A>G	GRCh37
NC_000019.8:g.9098541A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.86T>C MANE Select	ENSP00000302867.2:p.Met29Thr
NM_001001958.1:c.86T>C MANE Select	NP_001001958.1:p.Met29Thr