Canonical Allele Identifier: CA679597315
Gene: OR10A2 HGNC NCBI
OR2AG2 HGNC NCBI

Linked Data

dbSNP Id: rs1350099667
gnomAD v3: 11-6868432-C-G
gnomAD v4: 11-6868432-C-G
MyVariant Identifiers: chr11:g.6889663C>G (hg19) chr11:g.6868432C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6868432C>G , CM000673.2:g.6868432C>G GRCh38
NC_000011.9:g.6889663C>G , CM000673.1:g.6889663C>G GRCh37
NC_000011.8:g.6846239C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641461.1:c.-132-1191C>G (OR10A2) MANE Select ENSP00000493131.1:n.-132-1191C>G
XM_011520058.1:c.-436+29661G>C (OR2AG2) XP_011518360.1:n.-436+29661G>C
XM_011520059.1:c.-436+29661G>C (OR2AG2) XP_011518361.1:n.-436+29661G>C
XM_011520060.1:c.-436+29661G>C (OR2AG2) XP_011518362.1:n.-436+29661G>C
XM_011520061.1:c.-436+56066G>C (OR2AG2) XP_011518363.1:n.-436+56066G>C
NM_001004460.2:c.-132-1191C>G (OR10A2) MANE Select NP_001004460.1:n.-132-1191C>G
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