Canonical Allele Identifier: CA379433845
Gene: OR10A5 HGNC NCBI
OR2AG2 HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.6845726T>G
GRCh37 chr11:g.6866957T>G
Revel Score:
ENST00000299454 (MANE Select) 0.149
ENST00000379831 0.149
gnomAD v3:
11:6845726 T / G
gnomAD v4:
chr11-6845726-T-G
Joint Max Group AF 0.00433926 (NFE)
Genomes Max Group AF 0.00007341 (SAS)
Exomes Max Group AF 0.00461178 (NFE)
ClinVar Allele:
2264079
ClinVar RCV:
RCV004138089
ClinVar Variation:
2282039
dbSNP:
1848204060
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6845726T>G , CM000673.2:g.6845726T>G GRCh38
NC_000011.9:g.6866957T>G , CM000673.1:g.6866957T>G GRCh37
NC_000011.8:g.6823533T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000299454.5:c.44T>G (OR10A5) MANE Select ENSP00000299454.4:p.Met15Arg
ENST00000299454.4:c.44T>G (OR10A5) ENSP00000299454.4:p.Met15Arg
NM_178168.1:c.44T>G (OR10A5) MANE Select NP_835462.1:p.Met15Arg
XM_011520058.1:c.-436+52367A>C (OR2AG2) XP_011518360.1:n.-436+52367A>C
XM_011520059.1:c.-436+52367A>C (OR2AG2) XP_011518361.1:n.-436+52367A>C
XM_011520060.1:c.-436+52367A>C (OR2AG2) XP_011518362.1:n.-436+52367A>C
XM_011520061.1:c.-435-76235A>C (OR2AG2) XP_011518363.1:n.-435-76235A>C
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