Canonical Allele Identifier: CA217375803
Gene: OR10A2 HGNC NCBI
OR2AG2 HGNC NCBI

Linked Data

dbSNP Id: rs944499133
gnomAD v2: 11-6889659-TTCTCTATCCC-T
gnomAD v3: 11-6868428-TTCTCTATCCC-T
gnomAD v4: 11-6868428-TTCTCTATCCC-T
MyVariant Identifiers: chr11:g.6889660_6889669del (hg19) chr11:g.6868429_6868438del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6868429_6868438del , CM000673.2:g.6868429_6868438del GRCh38
NC_000011.9:g.6889660_6889669del , CM000673.1:g.6889660_6889669del GRCh37
NC_000011.8:g.6846236_6846245del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641461.1:c.-132-1194_-132-1185del (OR10A2) MANE Select ENSP00000493131.1:n.-132-1194_-132-1185del
XM_011520058.1:c.-436+29655_-436+29664del (OR2AG2) XP_011518360.1:n.-436+29655_-436+29664del
XM_011520059.1:c.-436+29655_-436+29664del (OR2AG2) XP_011518361.1:n.-436+29655_-436+29664del
XM_011520060.1:c.-436+29655_-436+29664del (OR2AG2) XP_011518362.1:n.-436+29655_-436+29664del
XM_011520061.1:c.-436+56060_-436+56069del (OR2AG2) XP_011518363.1:n.-436+56060_-436+56069del
NM_001004460.2:c.-132-1194_-132-1185del (OR10A2) MANE Select NP_001004460.1:n.-132-1194_-132-1185del
Search 100 bp 5'
Search 100 bp 3'