Canonical Allele Identifier: CA305051807

Gene: OR7G3

Linked Data

• ClinVar Variation Id: 2324750
• ClinVar RCV Id: RCV004165160
• dbSNP Id: rs1039892823
• gnomAD v2: 19-9237392-G-A
• gnomAD v3: 19-9126716-G-A
• gnomAD v4: 19-9126716-G-A
• MyVariant Identifiers: chr19:g.9237392G>A (hg19) ; chr19:g.9126716G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126716G>A , CM000681.2:g.9126716G>A	GRCh38
NC_000019.9:g.9237392G>A , CM000681.1:g.9237392G>A	GRCh37
NC_000019.8:g.9098392G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.235C>T MANE Select	ENSP00000302867.2:p.Pro79Ser
NM_001001958.1:c.235C>T MANE Select	NP_001001958.1:p.Pro79Ser