Canonical Allele Identifier: CA410111711

Gene: IFNGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33432184G>A , CM000683.2:g.33432184G>A	GRCh38
NC_000021.8:g.34804491G>A , CM000683.1:g.34804491G>A	GRCh37
NC_000021.7:g.33726361G>A	NCBI36
NG_007570.2:g.52193G>A , LRG_67:g.52193G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005534.4:c.569G>A MANE Select	NP_005525.2:p.Gly190Asp
ENST00000290219.11:c.569G>A MANE Select	ENSP00000290219.5:p.Gly190Asp
NM_001329128.1:c.626G>A	NP_001316057.1:p.Gly209Asp
NM_001329128.2:c.626G>A	NP_001316057.1:p.Gly209Asp
NM_005534.3:c.569G>A , LRG_67t1:c.569G>A	NP_005525.2:p.Gly190Asp
ENST00000290219.10:c.569G>A	ENSP00000290219.5:p.Gly190Asp
ENST00000381995.5:c.626G>A	ENSP00000371425.1:p.Gly209Asp
ENST00000405436.5:c.332G>A	ENSP00000385044.1:p.Gly111Asp
ENST00000439213.5:c.*544G>A	ENSP00000407541.1:n.*544G>A
ENST00000545369.2:c.*322G>A	ENSP00000442735.2:n.*322G>A
ENST00000696724.1:c.560G>A	ENSP00000512835.1:p.Gly187Asp
XM_005260969.2:c.626G>A	XP_005261026.1:p.Gly209Asp
XM_011529553.1:c.644G>A	XP_011527855.1:p.Gly215Asp
XM_011529554.1:c.575G>A	XP_011527856.1:p.Gly192Asp
XM_011529554.2:c.575G>A	XP_011527856.1:p.Gly192Asp