Canonical Allele Identifier: CA403790990

Gene: OR7G3

Linked Data

• MyVariant Identifiers: chr19:g.9237532A>C (hg19) ; chr19:g.9126856A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.9126856A>C , CM000681.2:g.9126856A>C	GRCh38
NC_000019.9:g.9237532A>C , CM000681.1:g.9237532A>C	GRCh37
NC_000019.8:g.9098532A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305444.2:c.95T>G MANE Select	ENSP00000302867.2:p.Leu32Arg
NM_001001958.1:c.95T>G MANE Select	NP_001001958.1:p.Leu32Arg