Canonical Allele Identifier: CA1950353288
Gene: OR10A2 HGNC NCBI
OR2AG2 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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