Canonical Allele Identifier: CA403788975

Gene: OR7G3

Linked Data

• dbSNP Id: rs371782613
• gnomAD v2: 19-9237336-G-T
• gnomAD v4: 19-9126660-G-T
• MyVariant Identifiers: chr19:g.9237336G>T (hg19) ; chr19:g.9126660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126660G>T , CM000681.2:g.9126660G>T	GRCh38
NC_000019.9:g.9237336G>T , CM000681.1:g.9237336G>T	GRCh37
NC_000019.8:g.9098336G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.291C>A MANE Select	ENSP00000302867.2:p.Cys97Ter
NM_001001958.1:c.291C>A MANE Select	NP_001001958.1:p.Cys97Ter