Canonical Allele Identifier: CA2480880302
Gene: IL6R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154465263_154465273delinsACCGGTGTCCC , CM000663.2:g.154465263_154465273delinsACCGGTGTCCC GRCh38
NC_000001.10:g.154437739_154437749delinsACCGGTGTCCC , CM000663.1:g.154437739_154437749delinsACCGGTGTCCC GRCh37
NC_000001.9:g.152704363_152704373delinsACCGGTGTCCC NCBI36
NG_012087.1:g.65071_65081delinsACCGGTGTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.1290_1300delinsACCGGTGTCCC MANE Select ENSP00000357470.3:p.Pro430=
ENST00000344086.8:c.*98_*108delinsACCGGTGTCCC ENSP00000340589.4:n.*98_*108delinsACCGGTGTCCC
ENST00000368485.7:c.1290_1300delinsACCGGTGTCCC ENSP00000357470.3:p.Pro430=
ENST00000507256.1:n.488_498delinsACCGGTGTCCC
NM_000565.3:c.1290_1300delinsACCGGTGTCCC NP_000556.1:p.Pro430=
NM_181359.2:c.*98_*108delinsACCGGTGTCCC NP_852004.1:n.*98_*108delinsACCGGTGTCCC
XM_005245139.1:c.1054_1064delinsACCGGTGTCCC XP_005245196.1:p.Thr352=
XM_005245140.1:c.*131_*141delinsACCGGTGTCCC XP_005245197.1:n.*131_*141delinsACCGGTGTCCC
XM_006711298.1:c.1338_1348delinsACCGGTGTCCC XP_006711361.1:p.Pro446=
XM_005245139.2:c.1054_1064delinsACCGGTGTCCC XP_005245196.1:p.Thr352=
XM_005245140.3:c.*131_*141delinsACCGGTGTCCC XP_005245197.1:n.*131_*141delinsACCGGTGTCCC
XM_006711298.2:c.1338_1348delinsACCGGTGTCCC XP_006711361.1:p.Pro446=
XM_017001199.2:c.1437_1447delinsACCGGTGTCCC XP_016856688.1:p.Pro479=
XM_017001200.2:c.1389_1399delinsACCGGTGTCCC XP_016856689.1:p.Pro463=
XM_017001201.2:c.*131_*141delinsACCGGTGTCCC XP_016856690.1:n.*131_*141delinsACCGGTGTCCC
NM_000565.4:c.1290_1300delinsACCGGTGTCCC MANE Select NP_000556.1:p.Pro430=
NM_181359.3:c.*98_*108delinsACCGGTGTCCC NP_852004.1:n.*98_*108delinsACCGGTGTCCC
NM_001382769.1:c.1389_1399delinsACCGGTGTCCC NP_001369698.1:p.Pro463=
NM_001382770.1:c.1383_1393delinsACCGGTGTCCC NP_001369699.1:p.Pro461=
NM_001382771.1:c.1338_1348delinsACCGGTGTCCC NP_001369700.1:p.Pro446=
NM_001382772.1:c.1284_1294delinsACCGGTGTCCC NP_001369701.1:p.Pro428=
NM_001382773.1:c.*98_*108delinsACCGGTGTCCC NP_001369702.1:n.*98_*108delinsACCGGTGTCCC
NM_001382774.1:c.930_940delinsACCGGTGTCCC NP_001369703.1:p.Pro310=