Canonical Allele Identifier: CA4018767

Gene: IFNGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137198160G>A , CM000668.2:g.137198160G>A	GRCh38
NC_000006.11:g.137519297G>A , CM000668.1:g.137519297G>A	GRCh37
NC_000006.10:g.137560990G>A	NCBI36
NG_007394.1:g.26271C>T , LRG_66:g.26271C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000416.3:c.1341C>T MANE Select	NP_000407.1:p.Thr447=
ENST00000367739.9:c.1341C>T MANE Select	ENSP00000356713.5:p.Thr447=
NM_000416.2:c.1341C>T , LRG_66t1:c.1341C>T	NP_000407.1:p.Thr447=
NM_001363526.1:c.1311C>T	NP_001350455.1:p.Thr437=
NM_001363527.1:c.1218C>T	NP_001350456.1:p.Thr406=
ENST00000367739.8:c.1341C>T	ENSP00000356713.4:p.Thr447=
ENST00000414770.6:c.1311C>T	ENSP00000394230.2:p.Thr437=
ENST00000458076.6:c.1239C>T	ENSP00000389249.2:p.Thr413=
ENST00000543628.5:c.*512C>T	ENSP00000443282.2:n.*512C>T
ENST00000642390.1:c.1284C>T	ENSP00000496468.1:p.Thr428=
ENST00000643119.1:c.1461C>T	ENSP00000495934.1:n.1461C>T
ENST00000644894.1:c.1218C>T	ENSP00000495272.1:p.Thr406=
ENST00000645045.1:c.1450C>T
ENST00000645753.1:c.1218C>T	ENSP00000495103.1:p.Thr406=
ENST00000646036.1:c.1311C>T	ENSP00000496387.1:p.Thr437=
ENST00000646898.1:c.1311C>T	ENSP00000494069.1:p.Thr437=
ENST00000647124.1:c.1218C>T	ENSP00000496549.1:p.Thr406=
ENST00000696693.1:c.1218C>T	ENSP00000512814.1:p.Thr406=
ENST00000696694.1:c.*439C>T	ENSP00000512815.1:n.*439C>T
ENST00000696695.1:c.1179C>T	ENSP00000512816.1:p.Thr393=
ENST00000696696.1:c.*1240C>T	ENSP00000512817.1:n.*1240C>T
ENST00000696697.1:c.1287C>T	ENSP00000512818.1:p.Thr429=
XM_006715470.2:c.1311C>T	XP_006715533.1:p.Thr437=
XM_006715470.3:c.1311C>T	XP_006715533.1:p.Thr437=
XM_006715471.2:c.1218C>T	XP_006715534.1:p.Thr406=
XM_011535793.1:c.1311C>T	XP_011534095.1:p.Thr437=
XM_011535793.2:c.1311C>T	XP_011534095.1:p.Thr437=
XM_011535794.1:c.1311C>T	XP_011534096.1:p.Thr437=