Canonical Allele Identifier: CA2480880388
Gene: IL6R HGNC NCBI

Linked Data

dbSNP Id: rs1691512777

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154465456_154465457insAGC , CM000663.2:g.154465456_154465457insAGC GRCh38
NC_000001.10:g.154437932_154437933insAGC , CM000663.1:g.154437932_154437933insAGC GRCh37
NC_000001.9:g.152704556_152704557insAGC NCBI36
NG_012087.1:g.65264_65265insAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.*76_*77insAGC MANE Select ENSP00000357470.3:n.*76_*77insAGC
ENST00000344086.8:c.*291_*292insAGC ENSP00000340589.4:n.*291_*292insAGC
ENST00000368485.7:c.*76_*77insAGC ENSP00000357470.3:n.*76_*77insAGC
NM_000565.3:c.*76_*77insAGC NP_000556.1:n.*76_*77insAGC
NM_181359.2:c.*291_*292insAGC NP_852004.1:n.*291_*292insAGC
XM_005245139.1:c.*164_*165insAGC XP_005245196.1:n.*164_*165insAGC
XM_005245140.1:c.*324_*325insAGC XP_005245197.1:n.*324_*325insAGC
XM_006711298.1:c.*76_*77insAGC XP_006711361.1:n.*76_*77insAGC
XM_005245139.2:c.*164_*165insAGC XP_005245196.1:n.*164_*165insAGC
XM_005245140.3:c.*324_*325insAGC XP_005245197.1:n.*324_*325insAGC
XM_006711298.2:c.*76_*77insAGC XP_006711361.1:n.*76_*77insAGC
XM_017001199.2:c.*76_*77insAGC XP_016856688.1:n.*76_*77insAGC
XM_017001200.2:c.*76_*77insAGC XP_016856689.1:n.*76_*77insAGC
XM_017001201.2:c.*324_*325insAGC XP_016856690.1:n.*324_*325insAGC
NM_000565.4:c.*76_*77insAGC MANE Select NP_000556.1:n.*76_*77insAGC
NM_181359.3:c.*291_*292insAGC NP_852004.1:n.*291_*292insAGC
NM_001382769.1:c.*76_*77insAGC NP_001369698.1:n.*76_*77insAGC
NM_001382770.1:c.*76_*77insAGC NP_001369699.1:n.*76_*77insAGC
NM_001382771.1:c.*76_*77insAGC NP_001369700.1:n.*76_*77insAGC
NM_001382772.1:c.*76_*77insAGC NP_001369701.1:n.*76_*77insAGC
NM_001382773.1:c.*291_*292insAGC NP_001369702.1:n.*291_*292insAGC
NM_001382774.1:c.*76_*77insAGC NP_001369703.1:n.*76_*77insAGC