Canonical Allele Identifier: CA485126033
Gene: OR11H7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.20698253A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20230094A>G , CM000676.2:g.20230094A>G GRCh38
NC_000014.8:g.20698253A>G , CM000676.1:g.20698253A>G GRCh37
NC_000014.7:g.19768093A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000553765.2:c.693A>G ENSP00000451021.2:p.Ser231=
ENST00000553765.1:c.693A>G ENSP00000451021.1:p.Ser231=
NM_001348273.1:c.693A>G MANE Select NP_001335202.1:p.Ser231=
NR_145509.1:n.1114A>G