Canonical Allele Identifier: CA2480880241

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465103_154465116delinsGTGTGGTTTGTCTT , CM000663.2:g.154465103_154465116delinsGTGTGGTTTGTCTT	GRCh38
NC_000001.10:g.154437579_154437592delinsGTGTGGTTTGTCTT , CM000663.1:g.154437579_154437592delinsGTGTGGTTTGTCTT	GRCh37
NC_000001.9:g.152704203_152704216delinsGTGTGGTTTGTCTT	NCBI36
NG_012087.1:g.64911_64924delinsGTGTGGTTTGTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1161-31_1161-18delinsGTGTGGTTTGTCTT MANE Select	ENSP00000357470.3:n.1161-31_1161-18delinsGTGTGGTTTGTCTT
ENST00000344086.8:c.1067-31_1067-18delinsGTGTGGTTTGTCTT	ENSP00000340589.4:n.1067-31_1067-18delinsGTGTGGTTTGTCTT
ENST00000368485.7:c.1161-31_1161-18delinsGTGTGGTTTGTCTT	ENSP00000357470.3:n.1161-31_1161-18delinsGTGTGGTTTGTCTT
ENST00000502679.1:n.474-31_474-18delinsGTGTGGTTTGTCTT
ENST00000507256.1:n.359-31_359-18delinsGTGTGGTTTGTCTT
NM_000565.3:c.1161-31_1161-18delinsGTGTGGTTTGTCTT	NP_000556.1:n.1161-31_1161-18delinsGTGTGGTTTGTCTT
NM_181359.2:c.1067-31_1067-18delinsGTGTGGTTTGTCTT	NP_852004.1:n.1067-31_1067-18delinsGTGTGGTTTGTCTT
XM_005245139.1:c.925-31_925-18delinsGTGTGGTTTGTCTT	XP_005245196.1:n.925-31_925-18delinsGTGTGGTTTGTCTT
XM_005245140.1:c.*2-31_*2-18delinsGTGTGGTTTGTCTT	XP_005245197.1:n.*2-31_*2-18delinsGTGTGGTTTGTCTT
XM_006711298.1:c.1209-31_1209-18delinsGTGTGGTTTGTCTT	XP_006711361.1:n.1209-31_1209-18delinsGTGTGGTTTGTCTT
XM_006711299.2:c.1115-31_1115-18delinsGTGTGGTTTGTCTT	XP_006711362.1:n.1115-31_1115-18delinsGTGTGGTTTGTCTT
XM_005245139.2:c.925-31_925-18delinsGTGTGGTTTGTCTT	XP_005245196.1:n.925-31_925-18delinsGTGTGGTTTGTCTT
XM_005245140.3:c.*2-31_*2-18delinsGTGTGGTTTGTCTT	XP_005245197.1:n.*2-31_*2-18delinsGTGTGGTTTGTCTT
XM_006711298.2:c.1209-31_1209-18delinsGTGTGGTTTGTCTT	XP_006711361.1:n.1209-31_1209-18delinsGTGTGGTTTGTCTT
XM_006711299.4:c.1115-31_1115-18delinsGTGTGGTTTGTCTT	XP_006711362.1:n.1115-31_1115-18delinsGTGTGGTTTGTCTT
XM_017001199.2:c.1308-31_1308-18delinsGTGTGGTTTGTCTT	XP_016856688.1:n.1308-31_1308-18delinsGTGTGGTTTGTCTT
XM_017001200.2:c.1260-31_1260-18delinsGTGTGGTTTGTCTT	XP_016856689.1:n.1260-31_1260-18delinsGTGTGGTTTGTCTT
XM_017001201.2:c.*2-31_*2-18delinsGTGTGGTTTGTCTT	XP_016856690.1:n.*2-31_*2-18delinsGTGTGGTTTGTCTT
NM_000565.4:c.1161-31_1161-18delinsGTGTGGTTTGTCTT MANE Select	NP_000556.1:n.1161-31_1161-18delinsGTGTGGTTTGTCTT
NM_181359.3:c.1067-31_1067-18delinsGTGTGGTTTGTCTT	NP_852004.1:n.1067-31_1067-18delinsGTGTGGTTTGTCTT
NM_001382769.1:c.1260-31_1260-18delinsGTGTGGTTTGTCTT	NP_001369698.1:n.1260-31_1260-18delinsGTGTGGTTTGTCTT
NM_001382770.1:c.1254-31_1254-18delinsGTGTGGTTTGTCTT	NP_001369699.1:n.1254-31_1254-18delinsGTGTGGTTTGTCTT
NM_001382771.1:c.1209-31_1209-18delinsGTGTGGTTTGTCTT	NP_001369700.1:n.1209-31_1209-18delinsGTGTGGTTTGTCTT
NM_001382772.1:c.1155-31_1155-18delinsGTGTGGTTTGTCTT	NP_001369701.1:n.1155-31_1155-18delinsGTGTGGTTTGTCTT
NM_001382773.1:c.1115-31_1115-18delinsGTGTGGTTTGTCTT	NP_001369702.1:n.1115-31_1115-18delinsGTGTGGTTTGTCTT
NM_001382774.1:c.801-31_801-18delinsGTGTGGTTTGTCTT	NP_001369703.1:n.801-31_801-18delinsGTGTGGTTTGTCTT