Canonical Allele Identifier: CA410093802
Gene: IFNAR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33241960T>G , CM000683.2:g.33241960T>G GRCh38
NC_000021.8:g.34614265T>G , CM000683.1:g.34614265T>G GRCh37
NC_000021.7:g.33536135T>G NCBI36
NG_016003.1:g.17035T>G
NG_016003.2:g.17035T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000433395.7:c.38T>G ENSP00000388223.3:p.Leu13Arg
ENST00000700427.1:n.248T>G
ENST00000700429.1:n.272T>G
ENST00000682009.1:c.38T>G ENSP00000506919.1:p.Leu13Arg
ENST00000683116.1:c.38T>G ENSP00000508125.1:p.Leu13Arg
ENST00000683941.1:c.38T>G ENSP00000508013.1:p.Leu13Arg
ENST00000342136.9:c.38T>G MANE Select ENSP00000343957.5:p.Leu13Arg
ENST00000646150.1:c.38T>G ENSP00000496248.1:p.Leu13Arg
ENST00000342101.7:c.38T>G ENSP00000343289.3:p.Leu13Arg
ENST00000342136.8:c.38T>G ENSP00000343957.4:p.Leu13Arg
ENST00000382238.6:c.38T>G ENSP00000371673.2:p.Leu13Arg
ENST00000382264.7:c.38T>G ENSP00000371699.3:p.Leu13Arg
ENST00000404220.7:c.38T>G ENSP00000384309.2:p.Leu13Arg
ENST00000413881.5:c.-119-2991T>G ENSP00000413160.1:n.-119-2991T>G
ENST00000420068.1:n.310T>G
ENST00000443073.5:c.-119-2991T>G ENSP00000403569.1:n.-119-2991T>G
ENST00000447980.1:c.110T>G ENSP00000402311.1:p.Leu37Arg
NM_000874.4:c.38T>G NP_000865.2:p.Leu13Arg
NM_001289125.1:c.38T>G NP_001276054.1:p.Leu13Arg
NM_001289126.1:c.38T>G NP_001276055.1:p.Leu13Arg
NM_001289128.1:c.38T>G NP_001276057.1:p.Leu13Arg
NM_207584.2:c.38T>G NP_997467.1:p.Leu13Arg
NM_207585.2:c.38T>G NP_997468.1:p.Leu13Arg
NM_000874.5:c.38T>G NP_000865.2:p.Leu13Arg
NM_001289125.3:c.38T>G MANE Select NP_001276054.1:p.Leu13Arg
NM_207584.3:c.38T>G NP_997467.1:p.Leu13Arg
NM_001289126.2:c.38T>G NP_001276055.1:p.Leu13Arg
NM_001289128.2:c.38T>G NP_001276057.1:p.Leu13Arg
NM_001385054.1:c.38T>G NP_001371983.1:p.Leu13Arg
NM_001385055.1:c.38T>G NP_001371984.1:p.Leu13Arg
NM_207585.3:c.38T>G NP_997468.1:p.Leu13Arg