Canonical Allele Identifier: CA678552787
Gene: OR2AH1P HGNC NCBI

Linked Data

dbSNP Id: rs1319415871
MyVariant Identifiers: chr11:g.56440102A>C (hg19) chr11:g.56672626A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.56672626A>C , CM000673.2:g.56672626A>C GRCh38
NC_000011.9:g.56440102A>C , CM000673.1:g.56440102A>C GRCh37
NC_000011.8:g.56196678A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641232.1:n.180-1206T>G
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