Canonical Allele Identifier: CA2121930460
Gene: OR11H7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20229992T= , CM000676.2:g.20229992T= GRCh38
NC_000014.8:g.20698151T= , CM000676.1:g.20698151T= GRCh37
NC_000014.7:g.19767991T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000553765.2:c.591T= ENSP00000451021.2:p.His197=
ENST00000553765.1:c.591T= ENSP00000451021.1:p.His197=
NM_001348273.1:c.591T= MANE Select NP_001335202.1:p.His197=
NR_145509.1:n.1012T=