Canonical Allele Identifier: CA599459420

Gene: OR2AH1P

Linked Data

• dbSNP Id: rs1305362596
• gnomAD v2: 11-56440145-C-A
• gnomAD v3: 11-56672669-C-A
• gnomAD v4: 11-56672669-C-A
• MyVariant Identifiers: chr11:g.56440145C>A (hg19) ; chr11:g.56672669C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.56672669C>A , CM000673.2:g.56672669C>A	GRCh38
NC_000011.9:g.56440145C>A , CM000673.1:g.56440145C>A	GRCh37
NC_000011.8:g.56196721C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641232.1:n.180-1249G>T