Canonical Allele Identifier: CA2746186217

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465601_154465608del , CM000663.2:g.154465601_154465608del	GRCh38
NC_000001.10:g.154438077_154438084del , CM000663.1:g.154438077_154438084del	GRCh37
NC_000001.9:g.152704701_152704708del	NCBI36
NG_012087.1:g.65409_65416del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*221_*228del MANE Select	ENSP00000357470.3:n.*221_*228del
ENST00000344086.8:c.*436_*443del	ENSP00000340589.4:n.*436_*443del
ENST00000368485.7:c.*221_*228del	ENSP00000357470.3:n.*221_*228del
NM_000565.3:c.*221_*228del	NP_000556.1:n.*221_*228del
NM_181359.2:c.*436_*443del	NP_852004.1:n.*436_*443del
XM_005245139.1:c.*309_*316del	XP_005245196.1:n.*309_*316del
XM_005245140.1:c.*469_*476del	XP_005245197.1:n.*469_*476del
XM_006711298.1:c.*221_*228del	XP_006711361.1:n.*221_*228del
XM_005245139.2:c.*309_*316del	XP_005245196.1:n.*309_*316del
XM_005245140.3:c.*469_*476del	XP_005245197.1:n.*469_*476del
XM_006711298.2:c.*221_*228del	XP_006711361.1:n.*221_*228del
XM_017001199.2:c.*221_*228del	XP_016856688.1:n.*221_*228del
XM_017001200.2:c.*221_*228del	XP_016856689.1:n.*221_*228del
XM_017001201.2:c.*469_*476del	XP_016856690.1:n.*469_*476del
NM_000565.4:c.*221_*228del MANE Select	NP_000556.1:n.*221_*228del
NM_181359.3:c.*436_*443del	NP_852004.1:n.*436_*443del
NM_001382769.1:c.*221_*228del	NP_001369698.1:n.*221_*228del
NM_001382770.1:c.*221_*228del	NP_001369699.1:n.*221_*228del
NM_001382771.1:c.*221_*228del	NP_001369700.1:n.*221_*228del
NM_001382772.1:c.*221_*228del	NP_001369701.1:n.*221_*228del
NM_001382773.1:c.*436_*443del	NP_001369702.1:n.*436_*443del
NM_001382774.1:c.*221_*228del	NP_001369703.1:n.*221_*228del