Canonical Allele Identifier: CA345612929

Gene: OR2M7

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.248324336A>T , CM000663.2:g.248324336A>T	GRCh38
NC_000001.10:g.248487638A>T , CM000663.1:g.248487638A>T	GRCh37
NC_000001.9:g.246554261A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317965.3:c.233T>A MANE Select	ENSP00000324557.2:p.Val78Glu
NM_001004691.1:c.233T>A MANE Select	NP_001004691.1:p.Val78Glu