Canonical Allele Identifier: CA222673836

Gene: OR2AH1P

Linked Data

• dbSNP Id: rs1001564979
• gnomAD v2: 11-56440071-C-G
• gnomAD v3: 11-56672595-C-G
• gnomAD v4: 11-56672595-C-G
• MyVariant Identifiers: chr11:g.56440071C>G (hg19) ; chr11:g.56672595C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.56672595C>G , CM000673.2:g.56672595C>G	GRCh38
NC_000011.9:g.56440071C>G , CM000673.1:g.56440071C>G	GRCh37
NC_000011.8:g.56196647C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641232.1:n.180-1175G>C