Canonical Allele Identifier: CA1666386027

Gene: IFNGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137206173G= , CM000668.2:g.137206173G=	GRCh38
NC_000006.11:g.137527310G= , CM000668.1:g.137527310G=	GRCh37
NC_000006.10:g.137569003G=	NCBI36
NG_007394.1:g.18258C= , LRG_66:g.18258C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414770.6:c.306C=	ENSP00000394230.2:p.Ala102=
ENST00000458076.6:c.234C=	ENSP00000389249.2:p.Ala78=
ENST00000696693.1:c.213C=	ENSP00000512814.1:p.Ala71=
ENST00000696694.1:c.336C=	ENSP00000512815.1:p.Ala112=
ENST00000696695.1:c.336C=	ENSP00000512816.1:p.Ala112=
ENST00000696696.1:c.*235C=	ENSP00000512817.1:n.*235C=
ENST00000696697.1:c.282C=	ENSP00000512818.1:p.Ala94=
ENST00000696698.1:c.336C=	ENSP00000512819.1:p.Ala112=
ENST00000696699.1:c.252C=	ENSP00000512820.1:p.Ala84=
ENST00000367739.9:c.336C= MANE Select	ENSP00000356713.5:p.Ala112=
ENST00000642390.1:c.279C=	ENSP00000496468.1:p.Ala93=
ENST00000643119.1:c.456C=	ENSP00000495934.1:n.456C=
ENST00000644894.1:c.213C=	ENSP00000495272.1:p.Ala71=
ENST00000645045.1:c.445C=
ENST00000645753.1:c.213C=	ENSP00000495103.1:p.Ala71=
ENST00000646036.1:c.306C=	ENSP00000496387.1:p.Ala102=
ENST00000646898.1:c.306C=	ENSP00000494069.1:p.Ala102=
ENST00000647124.1:c.213C=	ENSP00000496549.1:p.Ala71=
ENST00000367739.8:c.336C=	ENSP00000356713.4:p.Ala112=
ENST00000414770.5:c.306C=	ENSP00000394230.1:p.Ala102=
ENST00000458076.5:c.234C=	ENSP00000389249.1:p.Ala78=
ENST00000543628.5:c.336C=	ENSP00000443282.2:p.Ala112=
NM_000416.2:c.336C= , LRG_66t1:c.336C=	NP_000407.1:p.Ala112=
XM_006715470.2:c.306C=	XP_006715533.1:p.Ala102=
XM_006715471.2:c.213C=	XP_006715534.1:p.Ala71=
XM_011535793.1:c.306C=	XP_011534095.1:p.Ala102=
XM_011535794.1:c.306C=	XP_011534096.1:p.Ala102=
NM_001363526.1:c.306C=	NP_001350455.1:p.Ala102=
NM_001363527.1:c.213C=	NP_001350456.1:p.Ala71=
XM_006715470.3:c.306C=	XP_006715533.1:p.Ala102=
XM_011535793.2:c.306C=	XP_011534095.1:p.Ala102=
NM_000416.3:c.336C= MANE Select	NP_000407.1:p.Ala112=