Canonical Allele Identifier: CA1666386032

Gene: IFNGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137206190C= , CM000668.2:g.137206190C=	GRCh38
NC_000006.11:g.137527327C= , CM000668.1:g.137527327C=	GRCh37
NC_000006.10:g.137569020C=	NCBI36
NG_007394.1:g.18241G= , LRG_66:g.18241G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000414770.6:c.289G=	ENSP00000394230.2:p.Gly97=
ENST00000458076.6:c.217G=	ENSP00000389249.2:p.Gly73=
ENST00000696693.1:c.196G=	ENSP00000512814.1:p.Gly66=
ENST00000696694.1:c.319G=	ENSP00000512815.1:p.Gly107=
ENST00000696695.1:c.319G=	ENSP00000512816.1:p.Gly107=
ENST00000696696.1:c.*218G=	ENSP00000512817.1:n.*218G=
ENST00000696697.1:c.265G=	ENSP00000512818.1:p.Gly89=
ENST00000696698.1:c.319G=	ENSP00000512819.1:p.Gly107=
ENST00000696699.1:c.235G=	ENSP00000512820.1:p.Gly79=
ENST00000367739.9:c.319G= MANE Select	ENSP00000356713.5:p.Gly107=
ENST00000642390.1:c.262G=	ENSP00000496468.1:p.Gly88=
ENST00000643119.1:c.439G=	ENSP00000495934.1:n.439G=
ENST00000644894.1:c.196G=	ENSP00000495272.1:p.Gly66=
ENST00000645045.1:c.428G=
ENST00000645753.1:c.196G=	ENSP00000495103.1:p.Gly66=
ENST00000646036.1:c.289G=	ENSP00000496387.1:p.Gly97=
ENST00000646898.1:c.289G=	ENSP00000494069.1:p.Gly97=
ENST00000647124.1:c.196G=	ENSP00000496549.1:p.Gly66=
ENST00000367739.8:c.319G=	ENSP00000356713.4:p.Gly107=
ENST00000414770.5:c.289G=	ENSP00000394230.1:p.Gly97=
ENST00000458076.5:c.217G=	ENSP00000389249.1:p.Gly73=
ENST00000543628.5:c.319G=	ENSP00000443282.2:p.Gly107=
NM_000416.2:c.319G= , LRG_66t1:c.319G=	NP_000407.1:p.Gly107=
XM_006715470.2:c.289G=	XP_006715533.1:p.Gly97=
XM_006715471.2:c.196G=	XP_006715534.1:p.Gly66=
XM_011535793.1:c.289G=	XP_011534095.1:p.Gly97=
XM_011535794.1:c.289G=	XP_011534096.1:p.Gly97=
NM_001363526.1:c.289G=	NP_001350455.1:p.Gly97=
NM_001363527.1:c.196G=	NP_001350456.1:p.Gly66=
XM_006715470.3:c.289G=	XP_006715533.1:p.Gly97=
XM_011535793.2:c.289G=	XP_011534095.1:p.Gly97=
NM_000416.3:c.319G= MANE Select	NP_000407.1:p.Gly107=