Canonical Allele Identifier: CA597285875
Gene: OR10A2 HGNC NCBI
OR2AG2 HGNC NCBI

Linked Data

dbSNP Id: rs1331277143
gnomAD v2: 11-6889697-T-A
gnomAD v3: 11-6868466-T-A
gnomAD v4: 11-6868466-T-A
MyVariant Identifiers: chr11:g.6889697T>A (hg19) chr11:g.6868466T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6868466T>A , CM000673.2:g.6868466T>A GRCh38
NC_000011.9:g.6889697T>A , CM000673.1:g.6889697T>A GRCh37
NC_000011.8:g.6846273T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641461.1:c.-132-1157T>A (OR10A2) MANE Select ENSP00000493131.1:n.-132-1157T>A
XM_011520058.1:c.-436+29627A>T (OR2AG2) XP_011518360.1:n.-436+29627A>T
XM_011520059.1:c.-436+29627A>T (OR2AG2) XP_011518361.1:n.-436+29627A>T
XM_011520060.1:c.-436+29627A>T (OR2AG2) XP_011518362.1:n.-436+29627A>T
XM_011520061.1:c.-436+56032A>T (OR2AG2) XP_011518363.1:n.-436+56032A>T
NM_001004460.2:c.-132-1157T>A (OR10A2) MANE Select NP_001004460.1:n.-132-1157T>A
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