Canonical Allele Identifier: CA342628254
Gene: IL6R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154465144A>G , CM000663.2:g.154465144A>G GRCh38
NC_000001.10:g.154437620A>G , CM000663.1:g.154437620A>G GRCh37
NC_000001.9:g.152704244A>G NCBI36
NG_012087.1:g.64952A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.1171A>G MANE Select ENSP00000357470.3:p.Thr391Ala
ENST00000344086.8:c.1077A>G ENSP00000340589.4:p.Arg359=
ENST00000368485.7:c.1171A>G ENSP00000357470.3:p.Thr391Ala
ENST00000502679.1:n.484A>G
ENST00000507256.1:n.369A>G
NM_000565.3:c.1171A>G NP_000556.1:p.Thr391Ala
NM_181359.2:c.1077A>G NP_852004.1:p.Arg359=
XM_005245139.1:c.935A>G XP_005245196.1:p.Asp312Gly
XM_005245140.1:c.*12A>G XP_005245197.1:n.*12A>G
XM_006711298.1:c.1219A>G XP_006711361.1:p.Thr407Ala
XM_006711299.2:c.1125A>G XP_006711362.1:p.Arg375=
XM_005245139.2:c.935A>G XP_005245196.1:p.Asp312Gly
XM_005245140.3:c.*12A>G XP_005245197.1:n.*12A>G
XM_006711298.2:c.1219A>G XP_006711361.1:p.Thr407Ala
XM_006711299.4:c.1125A>G XP_006711362.1:p.Arg375=
XM_017001199.2:c.1318A>G XP_016856688.1:p.Thr440Ala
XM_017001200.2:c.1270A>G XP_016856689.1:p.Thr424Ala
XM_017001201.2:c.*12A>G XP_016856690.1:n.*12A>G
NM_000565.4:c.1171A>G MANE Select NP_000556.1:p.Thr391Ala
NM_181359.3:c.1077A>G NP_852004.1:p.Arg359=
NM_001382769.1:c.1270A>G NP_001369698.1:p.Thr424Ala
NM_001382770.1:c.1264A>G NP_001369699.1:p.Thr422Ala
NM_001382771.1:c.1219A>G NP_001369700.1:p.Thr407Ala
NM_001382772.1:c.1165A>G NP_001369701.1:p.Thr389Ala
NM_001382773.1:c.1125A>G NP_001369702.1:p.Arg375=
NM_001382774.1:c.811A>G NP_001369703.1:p.Thr271Ala