Canonical Allele Identifier: CA403786683
Gene: OR7G3 HGNC NCBI

Linked Data

gnomAD v4: 19-9126349-A-C
MyVariant Identifiers: chr19:g.9237025A>C (hg19) chr19:g.9126349A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126349A>C , CM000681.2:g.9126349A>C GRCh38
NC_000019.9:g.9237025A>C , CM000681.1:g.9237025A>C GRCh37
NC_000019.8:g.9098025A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.602T>G MANE Select ENSP00000302867.2:p.Leu201Trp
NM_001001958.1:c.602T>G MANE Select NP_001001958.1:p.Leu201Trp
Search 100 bp 5'
Search 100 bp 3'