Canonical Allele Identifier: CA9174494

Gene: OR7G3

Linked Data

• dbSNP Id: rs775795889
• ExAC: 19:9236965 A / G
• gnomAD v2: 19-9236965-A-G
• gnomAD v3: 19-9126289-A-G
• gnomAD v4: 19-9126289-A-G
• MyVariant Identifiers: chr19:g.9236965A>G (hg19) ; chr19:g.9126289A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126289A>G , CM000681.2:g.9126289A>G	GRCh38
NC_000019.9:g.9236965A>G , CM000681.1:g.9236965A>G	GRCh37
NC_000019.8:g.9097965A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.662T>C MANE Select	ENSP00000302867.2:p.Ile221Thr
NM_001001958.1:c.662T>C MANE Select	NP_001001958.1:p.Ile221Thr