Canonical Allele Identifier: CA1007944545

Gene: IL6R

Linked Data

• dbSNP Id: rs1691526098
• gnomAD v3: 1-154465764-G-C
• gnomAD v4: 1-154465764-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465764G>C , CM000663.2:g.154465764G>C	GRCh38
NC_000001.10:g.154438240G>C , CM000663.1:g.154438240G>C	GRCh37
NC_000001.9:g.152704864G>C	NCBI36
NG_012087.1:g.65572G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*384G>C MANE Select	ENSP00000357470.3:n.*384G>C
ENST00000344086.8:c.*599G>C	ENSP00000340589.4:n.*599G>C
ENST00000368485.7:c.*384G>C	ENSP00000357470.3:n.*384G>C
NM_000565.3:c.*384G>C	NP_000556.1:n.*384G>C
NM_181359.2:c.*599G>C	NP_852004.1:n.*599G>C
XM_005245139.1:c.*472G>C	XP_005245196.1:n.*472G>C
XM_005245140.1:c.*632G>C	XP_005245197.1:n.*632G>C
XM_006711298.1:c.*384G>C	XP_006711361.1:n.*384G>C
XM_005245139.2:c.*472G>C	XP_005245196.1:n.*472G>C
XM_005245140.3:c.*632G>C	XP_005245197.1:n.*632G>C
XM_006711298.2:c.*384G>C	XP_006711361.1:n.*384G>C
XM_017001199.2:c.*384G>C	XP_016856688.1:n.*384G>C
XM_017001200.2:c.*384G>C	XP_016856689.1:n.*384G>C
XM_017001201.2:c.*632G>C	XP_016856690.1:n.*632G>C
NM_000565.4:c.*384G>C MANE Select	NP_000556.1:n.*384G>C
NM_181359.3:c.*599G>C	NP_852004.1:n.*599G>C
NM_001382769.1:c.*384G>C	NP_001369698.1:n.*384G>C
NM_001382770.1:c.*384G>C	NP_001369699.1:n.*384G>C
NM_001382771.1:c.*384G>C	NP_001369700.1:n.*384G>C
NM_001382772.1:c.*384G>C	NP_001369701.1:n.*384G>C
NM_001382773.1:c.*599G>C	NP_001369702.1:n.*599G>C
NM_001382774.1:c.*384G>C	NP_001369703.1:n.*384G>C