Canonical Allele Identifier: CA403790206

Gene: OR7G3

Linked Data

• dbSNP Id: rs1159286647
• gnomAD v2: 19-9237455-G-A
• gnomAD v4: 19-9126779-G-A
• COSMIC: COSM6053122
• MyVariant Identifiers: chr19:g.9237455G>A (hg19) ; chr19:g.9126779G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126779G>A , CM000681.2:g.9126779G>A	GRCh38
NC_000019.9:g.9237455G>A , CM000681.1:g.9237455G>A	GRCh37
NC_000019.8:g.9098455G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.172C>T MANE Select	ENSP00000302867.2:p.Pro58Ser
NM_001001958.1:c.172C>T MANE Select	NP_001001958.1:p.Pro58Ser