Canonical Allele Identifier: CA505453032

Gene: OR7G3

Linked Data

• dbSNP Id: rs1319214849
• gnomAD v2: 19-9237075-A-G
• gnomAD v4: 19-9126399-A-G
• MyVariant Identifiers: chr19:g.9237075A>G (hg19) ; chr19:g.9126399A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126399A>G , CM000681.2:g.9126399A>G	GRCh38
NC_000019.9:g.9237075A>G , CM000681.1:g.9237075A>G	GRCh37
NC_000019.8:g.9098075A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.552T>C MANE Select	ENSP00000302867.2:p.Ile184=
NM_001001958.1:c.552T>C MANE Select	NP_001001958.1:p.Ile184=