Canonical Allele Identifier: CA403790181
Gene: OR7G3 HGNC NCBI

Linked Data

dbSNP Id: rs1460507853
gnomAD v2: 19-9237452-T-C
gnomAD v4: 19-9126776-T-C
MyVariant Identifiers: chr19:g.9237452T>C (hg19) chr19:g.9126776T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9126776T>C , CM000681.2:g.9126776T>C GRCh38
NC_000019.9:g.9237452T>C , CM000681.1:g.9237452T>C GRCh37
NC_000019.8:g.9098452T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305444.2:c.175A>G MANE Select ENSP00000302867.2:p.Met59Val
NM_001001958.1:c.175A>G MANE Select NP_001001958.1:p.Met59Val
Search 100 bp 5'
Search 100 bp 3'