Canonical Allele Identifier: CA2386671192

Gene: IFNGR2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33426974C= , CM000683.2:g.33426974C=	GRCh38
NC_000021.8:g.34799281C= , CM000683.1:g.34799281C=	GRCh37
NC_000021.7:g.33721151C=	NCBI36
NG_007570.2:g.46983C= , LRG_67:g.46983C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005534.4:c.503C= MANE Select	NP_005525.2:p.Thr168=
ENST00000290219.11:c.503C= MANE Select	ENSP00000290219.5:p.Thr168=
NM_001329128.1:c.560C=	NP_001316057.1:p.Thr187=
NM_001329128.2:c.560C=	NP_001316057.1:p.Thr187=
NM_005534.3:c.503C= , LRG_67t1:c.503C=	NP_005525.2:p.Thr168=
ENST00000290219.10:c.503C=	ENSP00000290219.5:p.Thr168=
ENST00000381995.5:c.560C=	ENSP00000371425.1:p.Thr187=
ENST00000405436.5:c.266C=	ENSP00000385044.1:p.Thr89=
ENST00000439213.5:c.*478C=	ENSP00000407541.1:n.*478C=
ENST00000545369.2:c.*256C=	ENSP00000442735.2:n.*256C=
ENST00000696724.1:c.494C=	ENSP00000512835.1:p.Thr165=
XM_005260969.2:c.560C=	XP_005261026.1:p.Thr187=
XM_011529553.1:c.578C=	XP_011527855.1:p.Thr193=
XM_011529554.1:c.509C=	XP_011527856.1:p.Thr170=
XM_011529554.2:c.509C=	XP_011527856.1:p.Thr170=