Canonical Allele Identifier: CA403789915

Gene: OR7G3

Linked Data

• gnomAD v3: 19-9126758-T-G
• gnomAD v4: 19-9126758-T-G
• MyVariant Identifiers: chr19:g.9237434T>G (hg19) ; chr19:g.9126758T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126758T>G , CM000681.2:g.9126758T>G	GRCh38
NC_000019.9:g.9237434T>G , CM000681.1:g.9237434T>G	GRCh37
NC_000019.8:g.9098434T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.193A>C MANE Select	ENSP00000302867.2:p.Ile65Leu
NM_001001958.1:c.193A>C MANE Select	NP_001001958.1:p.Ile65Leu