Canonical Allele Identifier: CA485125988
Gene: OR11H7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.20698239T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20230080T>G , CM000676.2:g.20230080T>G GRCh38
NC_000014.8:g.20698239T>G , CM000676.1:g.20698239T>G GRCh37
NC_000014.7:g.19768079T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000553765.2:c.679T>G ENSP00000451021.2:p.Ter227Glu
ENST00000553765.1:c.679T>G ENSP00000451021.1:p.Ter227Glu
NR_145509.1:n.1100T>G