Canonical Allele Identifier: CA222673936
Gene: OR2AH1P HGNC NCBI

Linked Data

dbSNP Id: rs985154336
MyVariant Identifiers: chr11:g.56440226C>T (hg19) chr11:g.56672750C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.56672750C>T , CM000673.2:g.56672750C>T GRCh38
NC_000011.9:g.56440226C>T , CM000673.1:g.56440226C>T GRCh37
NC_000011.8:g.56196802C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641232.1:n.180-1330G>A
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