Canonical Allele Identifier: CA374795288

Gene: OR1N2 OR1L8 OR1J2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122553380C>T , CM000671.2:g.122553380C>T	GRCh38
NC_000009.11:g.125315659C>T , CM000671.1:g.125315659C>T	GRCh37
NC_000009.10:g.124355480C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001004457.2:c.169C>T (OR1N2) MANE Select	NP_001004457.2:p.His57Tyr
ENST00000373688.3:c.169C>T (OR1N2) MANE Select	ENSP00000362792.3:p.His57Tyr
NM_001004457.1:c.211C>T (OR1N2)	NP_001004457.1:p.His71Tyr
ENST00000373688.2:c.211C>T (OR1N2)	ENSP00000362792.2:p.His71Tyr
ENST00000616791.1:c.157C>T (OR1N2)	ENSP00000483293.1:p.His53Tyr
ENST00000616791.3:c.157C>T (OR1N2)	ENSP00000483293.3:p.His53Tyr
XM_011518243.1:c.*23-6851G>A (OR1L8)	XP_011516545.1:n.*23-6851G>A
XM_017014285.1:c.*23-6851G>A (OR1L8)	XP_016869774.1:n.*23-6851G>A
XR_002956773.1:n.1915-26573C>T (OR1J2)
XR_929761.1:n.1915-26573C>T (OR1J2)