Canonical Allele Identifier: CA365776379

Gene: IFNGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137219242C>A , CM000668.2:g.137219242C>A	GRCh38
NC_000006.11:g.137540379C>A , CM000668.1:g.137540379C>A	GRCh37
NC_000006.10:g.137582072C>A	NCBI36
NG_007394.1:g.5189G>T , LRG_66:g.5189G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000416.3:c.85+1G>T MANE Select	NP_000407.1:n.85+1G>T
ENST00000367739.9:c.85+1G>T MANE Select	ENSP00000356713.5:n.85+1G>T
NM_000416.2:c.85+1G>T , LRG_66t1:c.85+1G>T	NP_000407.1:n.85+1G>T
ENST00000367739.8:c.85+1G>T	ENSP00000356713.4:n.85+1G>T
ENST00000414770.5:c.-57+1G>T	ENSP00000394230.1:n.-57+1G>T
ENST00000414770.6:c.-57+1G>T	ENSP00000394230.2:n.-57+1G>T
ENST00000458076.5:c.85+1G>T	ENSP00000389249.1:n.85+1G>T
ENST00000458076.6:c.85+1G>T	ENSP00000389249.2:n.85+1G>T
ENST00000478333.1:n.207+1G>T
ENST00000543628.5:c.85+1G>T	ENSP00000443282.2:n.85+1G>T
ENST00000643119.1:c.70+1G>T	ENSP00000495934.1:n.70+1G>T
ENST00000644894.1:c.-609G>T	ENSP00000495272.1:n.-609G>T
ENST00000645045.1:c.71+1G>T
ENST00000696694.1:c.85+1G>T	ENSP00000512815.1:n.85+1G>T
ENST00000696695.1:c.85+1G>T	ENSP00000512816.1:n.85+1G>T
ENST00000696696.1:c.85+1G>T	ENSP00000512817.1:n.85+1G>T
ENST00000696697.1:c.-163+1G>T	ENSP00000512818.1:n.-163+1G>T
ENST00000696698.1:c.85+1G>T	ENSP00000512819.1:n.85+1G>T
XM_011535793.1:c.-57+1G>T	XP_011534095.1:n.-57+1G>T
XM_011535793.2:c.-57+1G>T	XP_011534095.1:n.-57+1G>T