Canonical Allele Identifier: CA10908046
Gene: IL6R HGNC NCBI

Linked Data

dbSNP Id: rs7529229

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154448302T>C , CM000663.2:g.154448302T>C GRCh38
NC_000001.10:g.154420778T>C , CM000663.1:g.154420778T>C GRCh37
NC_000001.9:g.152687402T>C NCBI36
NG_012087.1:g.48110T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000368485.8:c.996+131T>C MANE Select ENSP00000357470.3:n.996+131T>C
ENST00000344086.8:c.996+131T>C ENSP00000340589.4:n.996+131T>C
ENST00000368485.7:c.996+131T>C ENSP00000357470.3:n.996+131T>C
ENST00000476006.5:n.812+131T>C
ENST00000507256.1:n.194+131T>C
ENST00000515190.1:n.404+131T>C
NM_000565.3:c.996+131T>C NP_000556.1:n.996+131T>C
NM_181359.2:c.996+131T>C NP_852004.1:n.996+131T>C
XM_005245139.1:c.854+131T>C XP_005245196.1:n.854+131T>C
XM_005245140.1:c.854+131T>C XP_005245197.1:n.854+131T>C
XM_006711298.1:c.1044+131T>C XP_006711361.1:n.1044+131T>C
XM_006711299.2:c.1044+131T>C XP_006711362.1:n.1044+131T>C
XM_005245139.2:c.854+131T>C XP_005245196.1:n.854+131T>C
XM_005245140.3:c.854+131T>C XP_005245197.1:n.854+131T>C
XM_006711298.2:c.1044+131T>C XP_006711361.1:n.1044+131T>C
XM_006711299.4:c.1044+131T>C XP_006711362.1:n.1044+131T>C
XM_017001199.2:c.1044+131T>C XP_016856688.1:n.1044+131T>C
XM_017001200.2:c.996+131T>C XP_016856689.1:n.996+131T>C
XM_017001201.2:c.854+131T>C XP_016856690.1:n.854+131T>C
NM_000565.4:c.996+131T>C MANE Select NP_000556.1:n.996+131T>C
NM_181359.3:c.996+131T>C NP_852004.1:n.996+131T>C
NM_001382769.1:c.996+131T>C NP_001369698.1:n.996+131T>C
NM_001382770.1:c.1089+131T>C NP_001369699.1:n.1089+131T>C
NM_001382771.1:c.1044+131T>C NP_001369700.1:n.1044+131T>C
NM_001382772.1:c.990+131T>C NP_001369701.1:n.990+131T>C
NM_001382773.1:c.1044+131T>C NP_001369702.1:n.1044+131T>C
NM_001382774.1:c.636+131T>C NP_001369703.1:n.636+131T>C