Canonical Allele Identifier: CA678552794

Gene: OR2AH1P

Linked Data

• dbSNP Id: rs11228718
• gnomAD v3: 11-56672653-C-A
• gnomAD v4: 11-56672653-C-A
• MyVariant Identifiers: chr11:g.56440129C>A (hg19) ; chr11:g.56672653C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.56672653C>A , CM000673.2:g.56672653C>A	GRCh38
NC_000011.9:g.56440129C>A , CM000673.1:g.56440129C>A	GRCh37
NC_000011.8:g.56196705C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641232.1:n.180-1233G>T