Canonical Allele Identifier: CA599459419

Gene: OR2AH1P

Linked Data

• dbSNP Id: rs1401659770
• gnomAD v2: 11-56440098-T-C
• gnomAD v3: 11-56672622-T-C
• gnomAD v4: 11-56672622-T-C
• MyVariant Identifiers: chr11:g.56440098T>C (hg19) ; chr11:g.56672622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.56672622T>C , CM000673.2:g.56672622T>C	GRCh38
NC_000011.9:g.56440098T>C , CM000673.1:g.56440098T>C	GRCh37
NC_000011.8:g.56196674T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641232.1:n.180-1202A>G