Canonical Allele Identifier: CA2648157178

Gene: IL6R

Linked Data

• gnomAD v4: 1-154465729-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465733dup , CM000663.2:g.154465733dup	GRCh38
NC_000001.10:g.154438209dup , CM000663.1:g.154438209dup	GRCh37
NC_000001.9:g.152704833dup	NCBI36
NG_012087.1:g.65541dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*353dup MANE Select	ENSP00000357470.3:n.*353dup
ENST00000344086.8:c.*568dup	ENSP00000340589.4:n.*568dup
ENST00000368485.7:c.*353dup	ENSP00000357470.3:n.*353dup
NM_000565.3:c.*353dup	NP_000556.1:n.*353dup
NM_181359.2:c.*568dup	NP_852004.1:n.*568dup
XM_005245139.1:c.*441dup	XP_005245196.1:n.*441dup
XM_005245140.1:c.*601dup	XP_005245197.1:n.*601dup
XM_006711298.1:c.*353dup	XP_006711361.1:n.*353dup
XM_005245139.2:c.*441dup	XP_005245196.1:n.*441dup
XM_005245140.3:c.*601dup	XP_005245197.1:n.*601dup
XM_006711298.2:c.*353dup	XP_006711361.1:n.*353dup
XM_017001199.2:c.*353dup	XP_016856688.1:n.*353dup
XM_017001200.2:c.*353dup	XP_016856689.1:n.*353dup
XM_017001201.2:c.*601dup	XP_016856690.1:n.*601dup
NM_000565.4:c.*353dup MANE Select	NP_000556.1:n.*353dup
NM_181359.3:c.*568dup	NP_852004.1:n.*568dup
NM_001382769.1:c.*353dup	NP_001369698.1:n.*353dup
NM_001382770.1:c.*353dup	NP_001369699.1:n.*353dup
NM_001382771.1:c.*353dup	NP_001369700.1:n.*353dup
NM_001382772.1:c.*353dup	NP_001369701.1:n.*353dup
NM_001382773.1:c.*568dup	NP_001369702.1:n.*568dup
NM_001382774.1:c.*353dup	NP_001369703.1:n.*353dup