Canonical Allele Identifier: CA365775615
Gene: IFNGR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137206153A>C , CM000668.2:g.137206153A>C GRCh38
NC_000006.11:g.137527290A>C , CM000668.1:g.137527290A>C GRCh37
NC_000006.10:g.137568983A>C NCBI36
NG_007394.1:g.18278T>G , LRG_66:g.18278T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000414770.6:c.326T>G ENSP00000394230.2:p.Phe109Cys
ENST00000458076.6:c.254T>G ENSP00000389249.2:p.Phe85Cys
ENST00000696693.1:c.233T>G ENSP00000512814.1:p.Phe78Cys
ENST00000696694.1:c.356T>G ENSP00000512815.1:p.Phe119Cys
ENST00000696695.1:c.356T>G ENSP00000512816.1:p.Phe119Cys
ENST00000696696.1:c.*255T>G ENSP00000512817.1:n.*255T>G
ENST00000696697.1:c.302T>G ENSP00000512818.1:p.Phe101Cys
ENST00000696698.1:c.356T>G ENSP00000512819.1:p.Phe119Cys
ENST00000696699.1:c.272T>G ENSP00000512820.1:p.Phe91Cys
ENST00000367739.9:c.356T>G MANE Select ENSP00000356713.5:p.Phe119Cys
ENST00000642390.1:c.299T>G ENSP00000496468.1:p.Phe100Cys
ENST00000643119.1:c.476T>G ENSP00000495934.1:n.476T>G
ENST00000644894.1:c.233T>G ENSP00000495272.1:p.Phe78Cys
ENST00000645045.1:c.465T>G
ENST00000645753.1:c.233T>G ENSP00000495103.1:p.Phe78Cys
ENST00000646036.1:c.326T>G ENSP00000496387.1:p.Phe109Cys
ENST00000646898.1:c.326T>G ENSP00000494069.1:p.Phe109Cys
ENST00000647124.1:c.233T>G ENSP00000496549.1:p.Phe78Cys
ENST00000367739.8:c.356T>G ENSP00000356713.4:p.Phe119Cys
ENST00000414770.5:c.326T>G ENSP00000394230.1:p.Phe109Cys
ENST00000458076.5:c.254T>G ENSP00000389249.1:p.Phe85Cys
ENST00000543628.5:c.356T>G ENSP00000443282.2:p.Phe119Cys
NM_000416.2:c.356T>G , LRG_66t1:c.356T>G NP_000407.1:p.Phe119Cys
XM_006715470.2:c.326T>G XP_006715533.1:p.Phe109Cys
XM_006715471.2:c.233T>G XP_006715534.1:p.Phe78Cys
XM_011535793.1:c.326T>G XP_011534095.1:p.Phe109Cys
XM_011535794.1:c.326T>G XP_011534096.1:p.Phe109Cys
NM_001363526.1:c.326T>G NP_001350455.1:p.Phe109Cys
NM_001363527.1:c.233T>G NP_001350456.1:p.Phe78Cys
XM_006715470.3:c.326T>G XP_006715533.1:p.Phe109Cys
XM_011535793.2:c.326T>G XP_011534095.1:p.Phe109Cys
NM_000416.3:c.356T>G MANE Select NP_000407.1:p.Phe119Cys