Canonical Allele Identifier: CA4019123

Gene: IFNGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137219348G>A , CM000668.2:g.137219348G>A	GRCh38
NC_000006.11:g.137540485G>A , CM000668.1:g.137540485G>A	GRCh37
NC_000006.10:g.137582178G>A	NCBI36
NG_007394.1:g.5083C>T , LRG_66:g.5083C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000416.3:c.-21C>T MANE Select	NP_000407.1:n.-21C>T
ENST00000367739.9:c.-21C>T MANE Select	ENSP00000356713.5:n.-21C>T
NM_000416.2:c.-21C>T , LRG_66t1:c.-21C>T	NP_000407.1:n.-21C>T
ENST00000367739.8:c.-21C>T	ENSP00000356713.4:n.-21C>T
ENST00000414770.5:c.-162C>T	ENSP00000394230.1:n.-162C>T
ENST00000414770.6:c.-162C>T	ENSP00000394230.2:n.-162C>T
ENST00000458076.5:c.-21C>T	ENSP00000389249.1:n.-21C>T
ENST00000458076.6:c.-21C>T	ENSP00000389249.2:n.-21C>T
ENST00000478333.1:n.102C>T
ENST00000543628.5:c.-21C>T	ENSP00000443282.2:n.-21C>T
ENST00000696694.1:c.-21C>T	ENSP00000512815.1:n.-21C>T
ENST00000696695.1:c.-21C>T	ENSP00000512816.1:n.-21C>T
ENST00000696696.1:c.-21C>T	ENSP00000512817.1:n.-21C>T
ENST00000696698.1:c.-21C>T	ENSP00000512819.1:n.-21C>T
XM_011535793.1:c.-162C>T	XP_011534095.1:n.-162C>T
XM_011535793.2:c.-162C>T	XP_011534095.1:n.-162C>T