Canonical Allele Identifier: CA305052051

Gene: OR7G3

Linked Data

• dbSNP Id: rs900120185
• gnomAD v2: 19-9237561-C-T
• gnomAD v3: 19-9126885-C-T
• gnomAD v4: 19-9126885-C-T
• MyVariant Identifiers: chr19:g.9237561C>T (hg19) ; chr19:g.9126885C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126885C>T , CM000681.2:g.9126885C>T	GRCh38
NC_000019.9:g.9237561C>T , CM000681.1:g.9237561C>T	GRCh37
NC_000019.8:g.9098561C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.66G>A MANE Select	ENSP00000302867.2:p.Glu22=
NM_001001958.1:c.66G>A MANE Select	NP_001001958.1:p.Glu22=