Canonical Allele Identifier: CA2648156804

Gene: IL6R

Linked Data

• gnomAD v4: 1-154465423-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465427_154465428del , CM000663.2:g.154465427_154465428del	GRCh38
NC_000001.10:g.154437903_154437904del , CM000663.1:g.154437903_154437904del	GRCh37
NC_000001.9:g.152704527_152704528del	NCBI36
NG_012087.1:g.65235_65236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*47_*48del MANE Select	ENSP00000357470.3:n.*47_*48del
ENST00000344086.8:c.*262_*263del	ENSP00000340589.4:n.*262_*263del
ENST00000368485.7:c.*47_*48del	ENSP00000357470.3:n.*47_*48del
NM_000565.3:c.*47_*48del	NP_000556.1:n.*47_*48del
NM_181359.2:c.*262_*263del	NP_852004.1:n.*262_*263del
XM_005245139.1:c.*135_*136del	XP_005245196.1:n.*135_*136del
XM_005245140.1:c.*295_*296del	XP_005245197.1:n.*295_*296del
XM_006711298.1:c.*47_*48del	XP_006711361.1:n.*47_*48del
XM_005245139.2:c.*135_*136del	XP_005245196.1:n.*135_*136del
XM_005245140.3:c.*295_*296del	XP_005245197.1:n.*295_*296del
XM_006711298.2:c.*47_*48del	XP_006711361.1:n.*47_*48del
XM_017001199.2:c.*47_*48del	XP_016856688.1:n.*47_*48del
XM_017001200.2:c.*47_*48del	XP_016856689.1:n.*47_*48del
XM_017001201.2:c.*295_*296del	XP_016856690.1:n.*295_*296del
NM_000565.4:c.*47_*48del MANE Select	NP_000556.1:n.*47_*48del
NM_181359.3:c.*262_*263del	NP_852004.1:n.*262_*263del
NM_001382769.1:c.*47_*48del	NP_001369698.1:n.*47_*48del
NM_001382770.1:c.*47_*48del	NP_001369699.1:n.*47_*48del
NM_001382771.1:c.*47_*48del	NP_001369700.1:n.*47_*48del
NM_001382772.1:c.*47_*48del	NP_001369701.1:n.*47_*48del
NM_001382773.1:c.*262_*263del	NP_001369702.1:n.*262_*263del
NM_001382774.1:c.*47_*48del	NP_001369703.1:n.*47_*48del