Canonical Allele Identifier: CA217375805
Gene: OR10A2 HGNC NCBI
OR2AG2 HGNC NCBI

Linked Data

dbSNP Id: rs1052715493
MyVariant Identifiers: chr11:g.6889717A>T (hg19) chr11:g.6868486A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6868486A>T , CM000673.2:g.6868486A>T GRCh38
NC_000011.9:g.6889717A>T , CM000673.1:g.6889717A>T GRCh37
NC_000011.8:g.6846293A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641461.1:c.-132-1137A>T (OR10A2) MANE Select ENSP00000493131.1:n.-132-1137A>T
XM_011520058.1:c.-436+29607T>A (OR2AG2) XP_011518360.1:n.-436+29607T>A
XM_011520059.1:c.-436+29607T>A (OR2AG2) XP_011518361.1:n.-436+29607T>A
XM_011520060.1:c.-436+29607T>A (OR2AG2) XP_011518362.1:n.-436+29607T>A
XM_011520061.1:c.-436+56012T>A (OR2AG2) XP_011518363.1:n.-436+56012T>A
NM_001004460.2:c.-132-1137A>T (OR10A2) MANE Select NP_001004460.1:n.-132-1137A>T
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