Canonical Allele Identifier: CA678552780

Gene: OR2AH1P

Linked Data

• dbSNP Id: rs1459459770
• gnomAD v3: 11-56672594-C-T
• gnomAD v4: 11-56672594-C-T
• MyVariant Identifiers: chr11:g.56440070C>T (hg19) ; chr11:g.56672594C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.56672594C>T , CM000673.2:g.56672594C>T	GRCh38
NC_000011.9:g.56440070C>T , CM000673.1:g.56440070C>T	GRCh37
NC_000011.8:g.56196646C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641232.1:n.180-1174G>A