Canonical Allele Identifier: CA2648156960

Gene: IL6R

Linked Data

• gnomAD v4: 1-154465579-TCCCTTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465581_154465587del , CM000663.2:g.154465581_154465587del	GRCh38
NC_000001.10:g.154438057_154438063del , CM000663.1:g.154438057_154438063del	GRCh37
NC_000001.9:g.152704681_152704687del	NCBI36
NG_012087.1:g.65389_65395del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*201_*207del MANE Select	ENSP00000357470.3:n.*201_*207del
ENST00000344086.8:c.*416_*422del	ENSP00000340589.4:n.*416_*422del
ENST00000368485.7:c.*201_*207del	ENSP00000357470.3:n.*201_*207del
NM_000565.3:c.*201_*207del	NP_000556.1:n.*201_*207del
NM_181359.2:c.*416_*422del	NP_852004.1:n.*416_*422del
XM_005245139.1:c.*289_*295del	XP_005245196.1:n.*289_*295del
XM_005245140.1:c.*449_*455del	XP_005245197.1:n.*449_*455del
XM_006711298.1:c.*201_*207del	XP_006711361.1:n.*201_*207del
XM_005245139.2:c.*289_*295del	XP_005245196.1:n.*289_*295del
XM_005245140.3:c.*449_*455del	XP_005245197.1:n.*449_*455del
XM_006711298.2:c.*201_*207del	XP_006711361.1:n.*201_*207del
XM_017001199.2:c.*201_*207del	XP_016856688.1:n.*201_*207del
XM_017001200.2:c.*201_*207del	XP_016856689.1:n.*201_*207del
XM_017001201.2:c.*449_*455del	XP_016856690.1:n.*449_*455del
NM_000565.4:c.*201_*207del MANE Select	NP_000556.1:n.*201_*207del
NM_181359.3:c.*416_*422del	NP_852004.1:n.*416_*422del
NM_001382769.1:c.*201_*207del	NP_001369698.1:n.*201_*207del
NM_001382770.1:c.*201_*207del	NP_001369699.1:n.*201_*207del
NM_001382771.1:c.*201_*207del	NP_001369700.1:n.*201_*207del
NM_001382772.1:c.*201_*207del	NP_001369701.1:n.*201_*207del
NM_001382773.1:c.*416_*422del	NP_001369702.1:n.*416_*422del
NM_001382774.1:c.*201_*207del	NP_001369703.1:n.*201_*207del