Canonical Allele Identifier: CA365775901
Gene: IFNGR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137206278G>C , CM000668.2:g.137206278G>C GRCh38
NC_000006.11:g.137527415G>C , CM000668.1:g.137527415G>C GRCh37
NC_000006.10:g.137569108G>C NCBI36
NG_007394.1:g.18153C>G , LRG_66:g.18153C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000414770.6:c.201C>G ENSP00000394230.2:p.Cys67Trp
ENST00000458076.6:c.201-72C>G ENSP00000389249.2:n.201-72C>G
ENST00000696693.1:c.108C>G ENSP00000512814.1:p.Cys36Trp
ENST00000696694.1:c.231C>G ENSP00000512815.1:p.Cys77Trp
ENST00000696695.1:c.231C>G ENSP00000512816.1:p.Cys77Trp
ENST00000696696.1:c.*130C>G ENSP00000512817.1:n.*130C>G
ENST00000696697.1:c.177C>G ENSP00000512818.1:p.Cys59Trp
ENST00000696698.1:c.231C>G ENSP00000512819.1:p.Cys77Trp
ENST00000696699.1:c.147C>G ENSP00000512820.1:p.Cys49Trp
ENST00000367739.9:c.231C>G MANE Select ENSP00000356713.5:p.Cys77Trp
ENST00000642390.1:c.174C>G ENSP00000496468.1:p.Cys58Trp
ENST00000643119.1:c.351C>G ENSP00000495934.1:n.351C>G
ENST00000644894.1:c.108C>G ENSP00000495272.1:p.Cys36Trp
ENST00000645045.1:c.340C>G
ENST00000645753.1:c.108C>G ENSP00000495103.1:p.Cys36Trp
ENST00000646036.1:c.201C>G ENSP00000496387.1:p.Cys67Trp
ENST00000646898.1:c.201C>G ENSP00000494069.1:p.Cys67Trp
ENST00000647124.1:c.108C>G ENSP00000496549.1:p.Cys36Trp
ENST00000367739.8:c.231C>G ENSP00000356713.4:p.Cys77Trp
ENST00000414770.5:c.201C>G ENSP00000394230.1:p.Cys67Trp
ENST00000458076.5:c.201-72C>G ENSP00000389249.1:n.201-72C>G
ENST00000543628.5:c.231C>G ENSP00000443282.2:p.Cys77Trp
NM_000416.2:c.231C>G , LRG_66t1:c.231C>G NP_000407.1:p.Cys77Trp
XM_006715470.2:c.201C>G XP_006715533.1:p.Cys67Trp
XM_006715471.2:c.108C>G XP_006715534.1:p.Cys36Trp
XM_011535793.1:c.201C>G XP_011534095.1:p.Cys67Trp
XM_011535794.1:c.201C>G XP_011534096.1:p.Cys67Trp
NM_001363526.1:c.201C>G NP_001350455.1:p.Cys67Trp
NM_001363527.1:c.108C>G NP_001350456.1:p.Cys36Trp
XM_006715470.3:c.201C>G XP_006715533.1:p.Cys67Trp
XM_011535793.2:c.201C>G XP_011534095.1:p.Cys67Trp
NM_000416.3:c.231C>G MANE Select NP_000407.1:p.Cys77Trp