Canonical Allele Identifier: CA403790846

Gene: OR7G3

Linked Data

• ClinVar Variation Id: 3206676
• ClinVar RCV Id: RCV004502059
• dbSNP Id: rs1246582286
• gnomAD v3: 19-9126841-G-A
• gnomAD v4: 19-9126841-G-A
• MyVariant Identifiers: chr19:g.9237517G>A (hg19) ; chr19:g.9126841G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126841G>A , CM000681.2:g.9126841G>A	GRCh38
NC_000019.9:g.9237517G>A , CM000681.1:g.9237517G>A	GRCh37
NC_000019.8:g.9098517G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.110C>T MANE Select	ENSP00000302867.2:p.Ala37Val
NM_001001958.1:c.110C>T MANE Select	NP_001001958.1:p.Ala37Val