Canonical Allele Identifier: CA403791622

Gene: OR7G3

Linked Data

• MyVariant Identifiers: chr19:g.9237589A>T (hg19) ; chr19:g.9126913A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126913A>T , CM000681.2:g.9126913A>T	GRCh38
NC_000019.9:g.9237589A>T , CM000681.1:g.9237589A>T	GRCh37
NC_000019.8:g.9098589A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.38T>A MANE Select	ENSP00000302867.2:p.Phe13Tyr
NM_001001958.1:c.38T>A MANE Select	NP_001001958.1:p.Phe13Tyr