Canonical Allele Identifier: CA1666389927

Gene: IFNGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137215318G= , CM000668.2:g.137215318G=	GRCh38
NC_000006.11:g.137536455G= , CM000668.1:g.137536455G=	GRCh37
NC_000006.10:g.137578148G=	NCBI36
NG_007394.1:g.9113C= , LRG_66:g.9113C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414770.6:c.4C=	ENSP00000394230.2:p.Leu2=
ENST00000458076.6:c.85+3925C=	ENSP00000389249.2:n.85+3925C=
ENST00000696693.1:c.-39+2710C=	ENSP00000512814.1:n.-39+2710C=
ENST00000696694.1:c.85+3925C=	ENSP00000512815.1:n.85+3925C=
ENST00000696695.1:c.85+3925C=	ENSP00000512816.1:n.85+3925C=
ENST00000696696.1:c.86-1486C=	ENSP00000512817.1:n.86-1486C=
ENST00000696697.1:c.-103C=	ENSP00000512818.1:n.-103C=
ENST00000696698.1:c.85+3925C=	ENSP00000512819.1:n.85+3925C=
ENST00000696699.1:c.1+3133C=	ENSP00000512820.1:n.1+3133C=
ENST00000367739.9:c.85+3925C= MANE Select	ENSP00000356713.5:n.85+3925C=
ENST00000642390.1:c.-96+3666C=	ENSP00000496468.1:n.-96+3666C=
ENST00000643119.1:c.70+3925C=	ENSP00000495934.1:n.70+3925C=
ENST00000644894.1:c.-39+3354C=	ENSP00000495272.1:n.-39+3354C=
ENST00000645045.1:c.71+3925C=
ENST00000645753.1:c.-39+3776C=	ENSP00000495103.1:n.-39+3776C=
ENST00000646036.1:c.4C=	ENSP00000496387.1:p.Leu2=
ENST00000646898.1:c.4C=	ENSP00000494069.1:p.Leu2=
ENST00000647124.1:c.-39+3666C=	ENSP00000496549.1:n.-39+3666C=
ENST00000367739.8:c.85+3925C=	ENSP00000356713.4:n.85+3925C=
ENST00000414770.5:c.4C=	ENSP00000394230.1:p.Leu2=
ENST00000458076.5:c.85+3925C=	ENSP00000389249.1:n.85+3925C=
ENST00000478333.1:n.207+3925C=
ENST00000543628.5:c.85+3925C=	ENSP00000443282.2:n.85+3925C=
NM_000416.2:c.85+3925C= , LRG_66t1:c.85+3925C=	NP_000407.1:n.85+3925C=
XM_006715470.2:c.4C=	XP_006715533.1:p.Leu2=
XM_006715471.2:c.-39+3354C=	XP_006715534.1:n.-39+3354C=
XM_011535793.1:c.4C=	XP_011534095.1:p.Leu2=
XM_011535794.1:c.4C=	XP_011534096.1:p.Leu2=
NM_001363526.1:c.4C=	NP_001350455.1:p.Leu2=
NM_001363527.1:c.-39+3354C=	NP_001350456.1:n.-39+3354C=
XM_006715470.3:c.4C=	XP_006715533.1:p.Leu2=
XM_011535793.2:c.4C=	XP_011534095.1:p.Leu2=
NM_000416.3:c.85+3925C= MANE Select	NP_000407.1:n.85+3925C=