Canonical Allele Identifier: CA148230757

Gene: IFNGR1

Linked Data

• dbSNP Id: rs867984641
• gnomAD v3: 6-137206057-G-T
• gnomAD v4: 6-137206057-G-T
• MyVariant Identifiers: chr6:g.137527194G>T (hg19) ; chr6:g.137206057G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137206057G>T , CM000668.2:g.137206057G>T	GRCh38
NC_000006.11:g.137527194G>T , CM000668.1:g.137527194G>T	GRCh37
NC_000006.10:g.137568887G>T	NCBI36
NG_007394.1:g.18374C>A , LRG_66:g.18374C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414770.6:c.343+79C>A	ENSP00000394230.2:n.343+79C>A
ENST00000458076.6:c.271+79C>A	ENSP00000389249.2:n.271+79C>A
ENST00000696693.1:c.250+79C>A	ENSP00000512814.1:n.250+79C>A
ENST00000696694.1:c.373+79C>A	ENSP00000512815.1:n.373+79C>A
ENST00000696695.1:c.373+79C>A	ENSP00000512816.1:n.373+79C>A
ENST00000696696.1:c.*272+79C>A	ENSP00000512817.1:n.*272+79C>A
ENST00000696697.1:c.319+79C>A	ENSP00000512818.1:n.319+79C>A
ENST00000696698.1:c.373+79C>A	ENSP00000512819.1:n.373+79C>A
ENST00000696699.1:c.289+79C>A	ENSP00000512820.1:n.289+79C>A
ENST00000367739.9:c.373+79C>A MANE Select	ENSP00000356713.5:n.373+79C>A
ENST00000642390.1:c.316+79C>A	ENSP00000496468.1:n.316+79C>A
ENST00000643119.1:c.493+79C>A	ENSP00000495934.1:n.493+79C>A
ENST00000644894.1:c.250+79C>A	ENSP00000495272.1:n.250+79C>A
ENST00000645045.1:c.482+79C>A
ENST00000645753.1:c.250+79C>A	ENSP00000495103.1:n.250+79C>A
ENST00000646036.1:c.343+79C>A	ENSP00000496387.1:n.343+79C>A
ENST00000646898.1:c.343+79C>A	ENSP00000494069.1:n.343+79C>A
ENST00000647124.1:c.250+79C>A	ENSP00000496549.1:n.250+79C>A
ENST00000367739.8:c.373+79C>A	ENSP00000356713.4:n.373+79C>A
ENST00000414770.5:c.343+79C>A	ENSP00000394230.1:n.343+79C>A
ENST00000458076.5:c.271+79C>A	ENSP00000389249.1:n.271+79C>A
ENST00000543628.5:c.373+79C>A	ENSP00000443282.2:n.373+79C>A
NM_000416.2:c.373+79C>A , LRG_66t1:c.373+79C>A	NP_000407.1:n.373+79C>A
XM_006715470.2:c.343+79C>A	XP_006715533.1:n.343+79C>A
XM_006715471.2:c.250+79C>A	XP_006715534.1:n.250+79C>A
XM_011535793.1:c.343+79C>A	XP_011534095.1:n.343+79C>A
XM_011535794.1:c.343+79C>A	XP_011534096.1:n.343+79C>A
NM_001363526.1:c.343+79C>A	NP_001350455.1:n.343+79C>A
NM_001363527.1:c.250+79C>A	NP_001350456.1:n.250+79C>A
XM_006715470.3:c.343+79C>A	XP_006715533.1:n.343+79C>A
XM_011535793.2:c.343+79C>A	XP_011534095.1:n.343+79C>A
NM_000416.3:c.373+79C>A MANE Select	NP_000407.1:n.373+79C>A