Canonical Allele Identifier: CA452236892
Gene: IFNGR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.137527298T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137206161T>A , CM000668.2:g.137206161T>A GRCh38
NC_000006.11:g.137527298T>A , CM000668.1:g.137527298T>A GRCh37
NC_000006.10:g.137568991T>A NCBI36
NG_007394.1:g.18270A>T , LRG_66:g.18270A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000414770.6:c.318A>T ENSP00000394230.2:p.Ser106=
ENST00000458076.6:c.246A>T ENSP00000389249.2:p.Ser82=
ENST00000696693.1:c.225A>T ENSP00000512814.1:p.Ser75=
ENST00000696694.1:c.348A>T ENSP00000512815.1:p.Ser116=
ENST00000696695.1:c.348A>T ENSP00000512816.1:p.Ser116=
ENST00000696696.1:c.*247A>T ENSP00000512817.1:n.*247A>T
ENST00000696697.1:c.294A>T ENSP00000512818.1:p.Ser98=
ENST00000696698.1:c.348A>T ENSP00000512819.1:p.Ser116=
ENST00000696699.1:c.264A>T ENSP00000512820.1:p.Ser88=
ENST00000367739.9:c.348A>T MANE Select ENSP00000356713.5:p.Ser116=
ENST00000642390.1:c.291A>T ENSP00000496468.1:p.Ser97=
ENST00000643119.1:c.468A>T ENSP00000495934.1:n.468A>T
ENST00000644894.1:c.225A>T ENSP00000495272.1:p.Ser75=
ENST00000645045.1:c.457A>T
ENST00000645753.1:c.225A>T ENSP00000495103.1:p.Ser75=
ENST00000646036.1:c.318A>T ENSP00000496387.1:p.Ser106=
ENST00000646898.1:c.318A>T ENSP00000494069.1:p.Ser106=
ENST00000647124.1:c.225A>T ENSP00000496549.1:p.Ser75=
ENST00000367739.8:c.348A>T ENSP00000356713.4:p.Ser116=
ENST00000414770.5:c.318A>T ENSP00000394230.1:p.Ser106=
ENST00000458076.5:c.246A>T ENSP00000389249.1:p.Ser82=
ENST00000543628.5:c.348A>T ENSP00000443282.2:p.Ser116=
NM_000416.2:c.348A>T , LRG_66t1:c.348A>T NP_000407.1:p.Ser116=
XM_006715470.2:c.318A>T XP_006715533.1:p.Ser106=
XM_006715471.2:c.225A>T XP_006715534.1:p.Ser75=
XM_011535793.1:c.318A>T XP_011534095.1:p.Ser106=
XM_011535794.1:c.318A>T XP_011534096.1:p.Ser106=
NM_001363526.1:c.318A>T NP_001350455.1:p.Ser106=
NM_001363527.1:c.225A>T NP_001350456.1:p.Ser75=
XM_006715470.3:c.318A>T XP_006715533.1:p.Ser106=
XM_011535793.2:c.318A>T XP_011534095.1:p.Ser106=
NM_000416.3:c.348A>T MANE Select NP_000407.1:p.Ser116=