Canonical Allele Identifier: CA2121930441
Gene: OR11H7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20229983C= , CM000676.2:g.20229983C= GRCh38
NC_000014.8:g.20698142C= , CM000676.1:g.20698142C= GRCh37
NC_000014.7:g.19767982C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000553765.2:c.582C= ENSP00000451021.2:p.Ile194=
ENST00000553765.1:c.582C= ENSP00000451021.1:p.Ile194=
NM_001348273.1:c.582C= MANE Select NP_001335202.1:p.Ile194=
NR_145509.1:n.1003C=