Canonical Allele Identifier: CA4019069
Gene: IFNGR1 HGNC NCBI

Linked Data

dbSNP Id: rs1327475

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137215318G>A , CM000668.2:g.137215318G>A GRCh38
NC_000006.11:g.137536455G>A , CM000668.1:g.137536455G>A GRCh37
NC_000006.10:g.137578148G>A NCBI36
NG_007394.1:g.9113C>T , LRG_66:g.9113C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000414770.6:c.4C>T ENSP00000394230.2:p.Leu2Phe
ENST00000458076.6:c.85+3925C>T ENSP00000389249.2:n.85+3925C>T
ENST00000696693.1:c.-39+2710C>T ENSP00000512814.1:n.-39+2710C>T
ENST00000696694.1:c.85+3925C>T ENSP00000512815.1:n.85+3925C>T
ENST00000696695.1:c.85+3925C>T ENSP00000512816.1:n.85+3925C>T
ENST00000696696.1:c.86-1486C>T ENSP00000512817.1:n.86-1486C>T
ENST00000696697.1:c.-103C>T ENSP00000512818.1:n.-103C>T
ENST00000696698.1:c.85+3925C>T ENSP00000512819.1:n.85+3925C>T
ENST00000696699.1:c.1+3133C>T ENSP00000512820.1:n.1+3133C>T
ENST00000367739.9:c.85+3925C>T MANE Select ENSP00000356713.5:n.85+3925C>T
ENST00000642390.1:c.-96+3666C>T ENSP00000496468.1:n.-96+3666C>T
ENST00000643119.1:c.70+3925C>T ENSP00000495934.1:n.70+3925C>T
ENST00000644894.1:c.-39+3354C>T ENSP00000495272.1:n.-39+3354C>T
ENST00000645045.1:c.71+3925C>T
ENST00000645753.1:c.-39+3776C>T ENSP00000495103.1:n.-39+3776C>T
ENST00000646036.1:c.4C>T ENSP00000496387.1:p.Leu2Phe
ENST00000646898.1:c.4C>T ENSP00000494069.1:p.Leu2Phe
ENST00000647124.1:c.-39+3666C>T ENSP00000496549.1:n.-39+3666C>T
ENST00000367739.8:c.85+3925C>T ENSP00000356713.4:n.85+3925C>T
ENST00000414770.5:c.4C>T ENSP00000394230.1:p.Leu2Phe
ENST00000458076.5:c.85+3925C>T ENSP00000389249.1:n.85+3925C>T
ENST00000478333.1:n.207+3925C>T
ENST00000543628.5:c.85+3925C>T ENSP00000443282.2:n.85+3925C>T
NM_000416.2:c.85+3925C>T , LRG_66t1:c.85+3925C>T NP_000407.1:n.85+3925C>T
XM_006715470.2:c.4C>T XP_006715533.1:p.Leu2Phe
XM_006715471.2:c.-39+3354C>T XP_006715534.1:n.-39+3354C>T
XM_011535793.1:c.4C>T XP_011534095.1:p.Leu2Phe
XM_011535794.1:c.4C>T XP_011534096.1:p.Leu2Phe
NM_001363526.1:c.4C>T NP_001350455.1:p.Leu2Phe
NM_001363527.1:c.-39+3354C>T NP_001350456.1:n.-39+3354C>T
XM_006715470.3:c.4C>T XP_006715533.1:p.Leu2Phe
XM_011535793.2:c.4C>T XP_011534095.1:p.Leu2Phe
NM_000416.3:c.85+3925C>T MANE Select NP_000407.1:n.85+3925C>T