Canonical Allele Identifier: CA380462249

Gene: OR5D14

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.55796268A>G , CM000673.2:g.55796268A>G	GRCh38
NC_000011.9:g.55563744A>G , CM000673.1:g.55563744A>G	GRCh37
NC_000011.8:g.55320320A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335605.1:c.713A>G MANE Select	ENSP00000334456.1:p.Lys238Arg
NM_001004735.1:c.713A>G MANE Select	NP_001004735.1:p.Lys238Arg