Canonical Allele Identifier: CA678552887

Gene: OR2AH1P

Linked Data

• dbSNP Id: rs1302598555
• gnomAD v3: 11-56672826-T-C
• gnomAD v4: 11-56672826-T-C
• MyVariant Identifiers: chr11:g.56440302T>C (hg19) ; chr11:g.56672826T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.56672826T>C , CM000673.2:g.56672826T>C	GRCh38
NC_000011.9:g.56440302T>C , CM000673.1:g.56440302T>C	GRCh37
NC_000011.8:g.56196878T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641232.1:n.179+1322A>G