ClinGen Allele Registry
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Canonical Allele Identifier:
CA222673868
Gene: OR2AH1P
HGNC
NCBI
Linked Data
dbSNP Id:
rs373275741
MyVariant Identifiers:
chr11:g.56440111T>C (hg19)
chr11:g.56672635T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.56672635T>C , CM000673.2:g.56672635T>C
GRCh38
NC_000011.9:g.56440111T>C , CM000673.1:g.56440111T>C
GRCh37
NC_000011.8:g.56196687T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000641232.1:n.180-1215A>G
Search 100 bp 5'
Search 100 bp 3'