Canonical Allele Identifier: CA222673927

Gene: OR2AH1P

Linked Data

• dbSNP Id: rs969664344
• gnomAD v2: 11-56440179-T-C
• gnomAD v3: 11-56672703-T-C
• gnomAD v4: 11-56672703-T-C
• MyVariant Identifiers: chr11:g.56440179T>C (hg19) ; chr11:g.56672703T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.56672703T>C , CM000673.2:g.56672703T>C	GRCh38
NC_000011.9:g.56440179T>C , CM000673.1:g.56440179T>C	GRCh37
NC_000011.8:g.56196755T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641232.1:n.180-1283A>G