Canonical Allele Identifier: CA10625889

Gene: IFNGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137197960C>A , CM000668.2:g.137197960C>A	GRCh38
NC_000006.11:g.137519097C>A , CM000668.1:g.137519097C>A	GRCh37
NC_000006.10:g.137560790C>A	NCBI36
NG_007394.1:g.26471G>T , LRG_66:g.26471G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000416.3:c.*71G>T MANE Select	NP_000407.1:n.*71G>T
ENST00000367739.9:c.*71G>T MANE Select	ENSP00000356713.5:n.*71G>T
NM_000416.2:c.*71G>T , LRG_66t1:c.*71G>T	NP_000407.1:n.*71G>T
NM_001363526.1:c.*71G>T	NP_001350455.1:n.*71G>T
NM_001363527.1:c.*71G>T	NP_001350456.1:n.*71G>T
ENST00000367739.8:c.*71G>T	ENSP00000356713.4:n.*71G>T
ENST00000414770.6:c.*71G>T	ENSP00000394230.2:n.*71G>T
ENST00000458076.6:c.*71G>T	ENSP00000389249.2:n.*71G>T
ENST00000543628.5:c.*712G>T	ENSP00000443282.2:n.*712G>T
ENST00000642390.1:c.*71G>T	ENSP00000496468.1:n.*71G>T
ENST00000643119.1:c.1661G>T	ENSP00000495934.1:n.1661G>T
ENST00000644894.1:c.*71G>T	ENSP00000495272.1:n.*71G>T
ENST00000645045.1:c.1650G>T
ENST00000645753.1:c.*71G>T	ENSP00000495103.1:n.*71G>T
ENST00000646036.1:c.*71G>T	ENSP00000496387.1:n.*71G>T
ENST00000646898.1:c.*71G>T	ENSP00000494069.1:n.*71G>T
ENST00000647124.1:c.*71G>T	ENSP00000496549.1:n.*71G>T
ENST00000696693.1:c.*71G>T	ENSP00000512814.1:n.*71G>T
ENST00000696694.1:c.*639G>T	ENSP00000512815.1:n.*639G>T
ENST00000696695.1:c.*71G>T	ENSP00000512816.1:n.*71G>T
ENST00000696696.1:c.*1440G>T	ENSP00000512817.1:n.*1440G>T
XM_006715470.2:c.*71G>T	XP_006715533.1:n.*71G>T
XM_006715470.3:c.*71G>T	XP_006715533.1:n.*71G>T
XM_006715471.2:c.*71G>T	XP_006715534.1:n.*71G>T
XM_011535793.1:c.*71G>T	XP_011534095.1:n.*71G>T
XM_011535793.2:c.*71G>T	XP_011534095.1:n.*71G>T
XM_011535794.1:c.*71G>T	XP_011534096.1:n.*71G>T