Canonical Allele Identifier: CA678552838

Gene: OR2AH1P

Linked Data

• dbSNP Id: rs1369702879
• gnomAD v3: 11-56672756-A-G
• gnomAD v4: 11-56672756-A-G
• MyVariant Identifiers: chr11:g.56440232A>G (hg19) ; chr11:g.56672756A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.56672756A>G , CM000673.2:g.56672756A>G	GRCh38
NC_000011.9:g.56440232A>G , CM000673.1:g.56440232A>G	GRCh37
NC_000011.8:g.56196808A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641232.1:n.180-1336T>C