Canonical Allele Identifier: CA403790482
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs779363807
gnomAD v2: 19-9237482-C-A
gnomAD v4: 19-9126806-C-A
MyVariant Identifiers: chr19:g.9237482C>A (hg19) chr19:g.9126806C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126806C>A , CM000681.2:g.9126806C>A GRCh38
NC_000019.9:g.9237482C>A , CM000681.1:g.9237482C>A GRCh37
NC_000019.8:g.9098482C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305444.2:c.145G>T MANE Select ENSP00000302867.2:p.Val49Phe
NM_001001958.1:c.145G>T MANE Select NP_001001958.1:p.Val49Phe
Search 100 bp 5'
Search 100 bp 3'