Canonical Allele Identifier: CA403786582
Gene: OR7G3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.9237010A>T (hg19) chr19:g.9126334A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126334A>T , CM000681.2:g.9126334A>T GRCh38
NC_000019.9:g.9237010A>T , CM000681.1:g.9237010A>T GRCh37
NC_000019.8:g.9098010A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.617T>A MANE Select ENSP00000302867.2:p.Leu206Ter
NM_001001958.1:c.617T>A MANE Select NP_001001958.1:p.Leu206Ter
Search 100 bp 5'
Search 100 bp 3'