Canonical Allele Identifier: CA6336280
Gene: OR10G4 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.124016035A>G
GRCh37 chr11:g.123886742A>G
Revel Score:
ENST00000320891 0.141
gnomAD v2:
11:123886742 A / G
gnomAD v3:
11:124016035 A / G
gnomAD v4:
chr11-124016035-A-G
Joint Max Group AF 0.00004369 (SAS)
Exomes Max Group AF 0.00003766 (SAS)
ClinVar RCV:
RCV004139883
ClinVar Variation:
2291800
dbSNP:
760450704
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.124016035A>G , CM000673.2:g.124016035A>G GRCh38
NC_000011.9:g.123886742A>G , CM000673.1:g.123886742A>G GRCh37
NC_000011.8:g.123391952A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641521.1:c.461A>G ENSP00000493354.1:p.His154Arg
ENST00000641722.1:c.461A>G MANE Select ENSP00000493036.1:p.His154Arg
ENST00000320891.4:c.461A>G ENSP00000325076.3:p.His154Arg
NM_001004462.1:c.461A>G NP_001004462.1:p.His154Arg
NM_001004462.2:c.461A>G MANE Select NP_001004462.1:p.His154Arg
Search 100 bp 5'
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