Canonical Allele Identifier: CA365775245

Gene: IFNGR1

Linked Data

• MyVariant Identifiers: chr6:g.137525499G>C (hg19) ; chr6:g.137204362G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137204362G>C , CM000668.2:g.137204362G>C	GRCh38
NC_000006.11:g.137525499G>C , CM000668.1:g.137525499G>C	GRCh37
NC_000006.10:g.137567192G>C	NCBI36
NG_007394.1:g.20069C>G , LRG_66:g.20069C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000414770.6:c.486C>G	ENSP00000394230.2:p.Tyr162Ter
ENST00000458076.6:c.414C>G	ENSP00000389249.2:p.Tyr138Ter
ENST00000696693.1:c.393C>G	ENSP00000512814.1:p.Tyr131Ter
ENST00000696694.1:c.516C>G	ENSP00000512815.1:p.Tyr172Ter
ENST00000696695.1:c.516C>G	ENSP00000512816.1:p.Tyr172Ter
ENST00000696696.1:c.*415C>G	ENSP00000512817.1:n.*415C>G
ENST00000696697.1:c.462C>G	ENSP00000512818.1:p.Tyr154Ter
ENST00000696698.1:c.516C>G	ENSP00000512819.1:p.Tyr172Ter
ENST00000696699.1:c.432C>G	ENSP00000512820.1:p.Tyr144Ter
ENST00000367739.9:c.516C>G MANE Select	ENSP00000356713.5:p.Tyr172Ter
ENST00000642390.1:c.459C>G	ENSP00000496468.1:p.Tyr153Ter
ENST00000643119.1:c.636C>G	ENSP00000495934.1:n.636C>G
ENST00000644894.1:c.393C>G	ENSP00000495272.1:p.Tyr131Ter
ENST00000645045.1:c.625C>G
ENST00000645753.1:c.393C>G	ENSP00000495103.1:p.Tyr131Ter
ENST00000646036.1:c.486C>G	ENSP00000496387.1:p.Tyr162Ter
ENST00000646898.1:c.486C>G	ENSP00000494069.1:p.Tyr162Ter
ENST00000647124.1:c.393C>G	ENSP00000496549.1:p.Tyr131Ter
ENST00000367739.8:c.516C>G	ENSP00000356713.4:p.Tyr172Ter
ENST00000458076.5:c.414C>G	ENSP00000389249.1:p.Tyr138Ter
ENST00000543628.5:c.516C>G	ENSP00000443282.2:p.Tyr172Ter
NM_000416.2:c.516C>G , LRG_66t1:c.516C>G	NP_000407.1:p.Tyr172Ter
XM_006715470.2:c.486C>G	XP_006715533.1:p.Tyr162Ter
XM_006715471.2:c.393C>G	XP_006715534.1:p.Tyr131Ter
XM_011535793.1:c.486C>G	XP_011534095.1:p.Tyr162Ter
XM_011535794.1:c.486C>G	XP_011534096.1:p.Tyr162Ter
NM_001363526.1:c.486C>G	NP_001350455.1:p.Tyr162Ter
NM_001363527.1:c.393C>G	NP_001350456.1:p.Tyr131Ter
XM_006715470.3:c.486C>G	XP_006715533.1:p.Tyr162Ter
XM_011535793.2:c.486C>G	XP_011534095.1:p.Tyr162Ter
NM_000416.3:c.516C>G MANE Select	NP_000407.1:p.Tyr172Ter