Canonical Allele Identifier: CA365775669

Gene: IFNGR1

Linked Data

• MyVariant Identifiers: chr6:g.137527312C>A (hg19) ; chr6:g.137206175C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137206175C>A , CM000668.2:g.137206175C>A	GRCh38
NC_000006.11:g.137527312C>A , CM000668.1:g.137527312C>A	GRCh37
NC_000006.10:g.137569005C>A	NCBI36
NG_007394.1:g.18256G>T , LRG_66:g.18256G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414770.6:c.304G>T	ENSP00000394230.2:p.Ala102Ser
ENST00000458076.6:c.232G>T	ENSP00000389249.2:p.Ala78Ser
ENST00000696693.1:c.211G>T	ENSP00000512814.1:p.Ala71Ser
ENST00000696694.1:c.334G>T	ENSP00000512815.1:p.Ala112Ser
ENST00000696695.1:c.334G>T	ENSP00000512816.1:p.Ala112Ser
ENST00000696696.1:c.*233G>T	ENSP00000512817.1:n.*233G>T
ENST00000696697.1:c.280G>T	ENSP00000512818.1:p.Ala94Ser
ENST00000696698.1:c.334G>T	ENSP00000512819.1:p.Ala112Ser
ENST00000696699.1:c.250G>T	ENSP00000512820.1:p.Ala84Ser
ENST00000367739.9:c.334G>T MANE Select	ENSP00000356713.5:p.Ala112Ser
ENST00000642390.1:c.277G>T	ENSP00000496468.1:p.Ala93Ser
ENST00000643119.1:c.454G>T	ENSP00000495934.1:n.454G>T
ENST00000644894.1:c.211G>T	ENSP00000495272.1:p.Ala71Ser
ENST00000645045.1:c.443G>T
ENST00000645753.1:c.211G>T	ENSP00000495103.1:p.Ala71Ser
ENST00000646036.1:c.304G>T	ENSP00000496387.1:p.Ala102Ser
ENST00000646898.1:c.304G>T	ENSP00000494069.1:p.Ala102Ser
ENST00000647124.1:c.211G>T	ENSP00000496549.1:p.Ala71Ser
ENST00000367739.8:c.334G>T	ENSP00000356713.4:p.Ala112Ser
ENST00000414770.5:c.304G>T	ENSP00000394230.1:p.Ala102Ser
ENST00000458076.5:c.232G>T	ENSP00000389249.1:p.Ala78Ser
ENST00000543628.5:c.334G>T	ENSP00000443282.2:p.Ala112Ser
NM_000416.2:c.334G>T , LRG_66t1:c.334G>T	NP_000407.1:p.Ala112Ser
XM_006715470.2:c.304G>T	XP_006715533.1:p.Ala102Ser
XM_006715471.2:c.211G>T	XP_006715534.1:p.Ala71Ser
XM_011535793.1:c.304G>T	XP_011534095.1:p.Ala102Ser
XM_011535794.1:c.304G>T	XP_011534096.1:p.Ala102Ser
NM_001363526.1:c.304G>T	NP_001350455.1:p.Ala102Ser
NM_001363527.1:c.211G>T	NP_001350456.1:p.Ala71Ser
XM_006715470.3:c.304G>T	XP_006715533.1:p.Ala102Ser
XM_011535793.2:c.304G>T	XP_011534095.1:p.Ala102Ser
NM_000416.3:c.334G>T MANE Select	NP_000407.1:p.Ala112Ser