Canonical Allele Identifier: CA222673831
Gene: OR2AH1P HGNC NCBI

Linked Data

dbSNP Id: rs905939972
gnomAD v3: 11-56672579-G-A
gnomAD v4: 11-56672579-G-A
MyVariant Identifiers: chr11:g.56440055G>A (hg19) chr11:g.56672579G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.56672579G>A , CM000673.2:g.56672579G>A GRCh38
NC_000011.9:g.56440055G>A , CM000673.1:g.56440055G>A GRCh37
NC_000011.8:g.56196631G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641232.1:n.180-1159C>T
Search 100 bp 5'
Search 100 bp 3'