Canonical Allele Identifier: CA452236899
Gene: IFNGR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.137527310G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.137206173G>C , CM000668.2:g.137206173G>C GRCh38
NC_000006.11:g.137527310G>C , CM000668.1:g.137527310G>C GRCh37
NC_000006.10:g.137569003G>C NCBI36
NG_007394.1:g.18258C>G , LRG_66:g.18258C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000414770.6:c.306C>G ENSP00000394230.2:p.Ala102=
ENST00000458076.6:c.234C>G ENSP00000389249.2:p.Ala78=
ENST00000696693.1:c.213C>G ENSP00000512814.1:p.Ala71=
ENST00000696694.1:c.336C>G ENSP00000512815.1:p.Ala112=
ENST00000696695.1:c.336C>G ENSP00000512816.1:p.Ala112=
ENST00000696696.1:c.*235C>G ENSP00000512817.1:n.*235C>G
ENST00000696697.1:c.282C>G ENSP00000512818.1:p.Ala94=
ENST00000696698.1:c.336C>G ENSP00000512819.1:p.Ala112=
ENST00000696699.1:c.252C>G ENSP00000512820.1:p.Ala84=
ENST00000367739.9:c.336C>G MANE Select ENSP00000356713.5:p.Ala112=
ENST00000642390.1:c.279C>G ENSP00000496468.1:p.Ala93=
ENST00000643119.1:c.456C>G ENSP00000495934.1:n.456C>G
ENST00000644894.1:c.213C>G ENSP00000495272.1:p.Ala71=
ENST00000645045.1:c.445C>G
ENST00000645753.1:c.213C>G ENSP00000495103.1:p.Ala71=
ENST00000646036.1:c.306C>G ENSP00000496387.1:p.Ala102=
ENST00000646898.1:c.306C>G ENSP00000494069.1:p.Ala102=
ENST00000647124.1:c.213C>G ENSP00000496549.1:p.Ala71=
ENST00000367739.8:c.336C>G ENSP00000356713.4:p.Ala112=
ENST00000414770.5:c.306C>G ENSP00000394230.1:p.Ala102=
ENST00000458076.5:c.234C>G ENSP00000389249.1:p.Ala78=
ENST00000543628.5:c.336C>G ENSP00000443282.2:p.Ala112=
NM_000416.2:c.336C>G , LRG_66t1:c.336C>G NP_000407.1:p.Ala112=
XM_006715470.2:c.306C>G XP_006715533.1:p.Ala102=
XM_006715471.2:c.213C>G XP_006715534.1:p.Ala71=
XM_011535793.1:c.306C>G XP_011534095.1:p.Ala102=
XM_011535794.1:c.306C>G XP_011534096.1:p.Ala102=
NM_001363526.1:c.306C>G NP_001350455.1:p.Ala102=
NM_001363527.1:c.213C>G NP_001350456.1:p.Ala71=
XM_006715470.3:c.306C>G XP_006715533.1:p.Ala102=
XM_011535793.2:c.306C>G XP_011534095.1:p.Ala102=
NM_000416.3:c.336C>G MANE Select NP_000407.1:p.Ala112=