Canonical Allele Identifier: CA403791767

Gene: OR7G3

Linked Data

• dbSNP Id: rs1197384227
• gnomAD v3: 19-9126925-G-T
• gnomAD v4: 19-9126925-G-T
• MyVariant Identifiers: chr19:g.9237601G>T (hg19) ; chr19:g.9126925G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126925G>T , CM000681.2:g.9126925G>T	GRCh38
NC_000019.9:g.9237601G>T , CM000681.1:g.9237601G>T	GRCh37
NC_000019.8:g.9098601G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.26C>A MANE Select	ENSP00000302867.2:p.Thr9Asn
NM_001001958.1:c.26C>A MANE Select	NP_001001958.1:p.Thr9Asn