Canonical Allele Identifier: CA2386584957
Gene: IFNAR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33241734G= , CM000683.2:g.33241734G= GRCh38
NC_000021.8:g.34614039G= , CM000683.1:g.34614039G= GRCh37
NC_000021.7:g.33535909G= NCBI36
NG_016003.1:g.16809G=
NG_016003.2:g.16809G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433395.7:c.-37-152G= ENSP00000388223.3:n.-37-152G=
ENST00000700427.1:n.174-152G=
ENST00000700429.1:n.152-106G=
ENST00000682009.1:c.-37-152G= ENSP00000506919.1:n.-37-152G=
ENST00000683116.1:c.-37-152G= ENSP00000508125.1:n.-37-152G=
ENST00000683941.1:c.-83-106G= ENSP00000508013.1:n.-83-106G=
ENST00000342136.9:c.-83-106G= MANE Select ENSP00000343957.5:n.-83-106G=
ENST00000646150.1:c.-37-152G= ENSP00000496248.1:n.-37-152G=
ENST00000342101.7:c.-83-106G= ENSP00000343289.3:n.-83-106G=
ENST00000342136.8:c.-83-106G= ENSP00000343957.4:n.-83-106G=
ENST00000382238.6:c.-37-152G= ENSP00000371673.2:n.-37-152G=
ENST00000382264.7:c.-37-152G= ENSP00000371699.3:n.-37-152G=
ENST00000404220.7:c.-83-106G= ENSP00000384309.2:n.-83-106G=
ENST00000413881.5:c.-119-3217G= ENSP00000413160.1:n.-119-3217G=
ENST00000420068.1:n.236-152G=
ENST00000443073.5:c.-119-3217G= ENSP00000403569.1:n.-119-3217G=
ENST00000447980.1:c.36-152G= ENSP00000402311.1:n.36-152G=
NM_000874.4:c.-83-106G= NP_000865.2:n.-83-106G=
NM_001289125.1:c.-83-106G= NP_001276054.1:n.-83-106G=
NM_001289126.1:c.-37-152G= NP_001276055.1:n.-37-152G=
NM_001289128.1:c.-83-106G= NP_001276057.1:n.-83-106G=
NM_207584.2:c.-37-152G= NP_997467.1:n.-37-152G=
NM_207585.2:c.-37-152G= NP_997468.1:n.-37-152G=
NM_000874.5:c.-83-106G= NP_000865.2:n.-83-106G=
NM_001289125.3:c.-83-106G= MANE Select NP_001276054.1:n.-83-106G=
NM_207584.3:c.-37-152G= NP_997467.1:n.-37-152G=
NM_001289126.2:c.-37-152G= NP_001276055.1:n.-37-152G=
NM_001289128.2:c.-83-106G= NP_001276057.1:n.-83-106G=
NM_001385054.1:c.-37-152G= NP_001371983.1:n.-37-152G=
NM_001385055.1:c.-37-152G= NP_001371984.1:n.-37-152G=
NM_207585.3:c.-37-152G= NP_997468.1:n.-37-152G=