Canonical Allele Identifier: CA889598661

Gene: IL6R

Linked Data

• dbSNP Id: rs1328040931
• MyVariant Identifiers: chr1:g.154438254_154438258del (hg19) ; chr1:g.154465778_154465782del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465778_154465782del , CM000663.2:g.154465778_154465782del	GRCh38
NC_000001.10:g.154438254_154438258del , CM000663.1:g.154438254_154438258del	GRCh37
NC_000001.9:g.152704878_152704882del	NCBI36
NG_012087.1:g.65586_65590del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*398_*402del MANE Select	ENSP00000357470.3:n.*398_*402del
ENST00000344086.8:c.*613_*617del	ENSP00000340589.4:n.*613_*617del
ENST00000368485.7:c.*398_*402del	ENSP00000357470.3:n.*398_*402del
NM_000565.3:c.*398_*402del	NP_000556.1:n.*398_*402del
NM_181359.2:c.*613_*617del	NP_852004.1:n.*613_*617del
XM_005245139.1:c.*486_*490del	XP_005245196.1:n.*486_*490del
XM_005245140.1:c.*646_*650del	XP_005245197.1:n.*646_*650del
XM_006711298.1:c.*398_*402del	XP_006711361.1:n.*398_*402del
XM_005245139.2:c.*486_*490del	XP_005245196.1:n.*486_*490del
XM_005245140.3:c.*646_*650del	XP_005245197.1:n.*646_*650del
XM_006711298.2:c.*398_*402del	XP_006711361.1:n.*398_*402del
XM_017001199.2:c.*398_*402del	XP_016856688.1:n.*398_*402del
XM_017001200.2:c.*398_*402del	XP_016856689.1:n.*398_*402del
XM_017001201.2:c.*646_*650del	XP_016856690.1:n.*646_*650del
NM_000565.4:c.*398_*402del MANE Select	NP_000556.1:n.*398_*402del
NM_181359.3:c.*613_*617del	NP_852004.1:n.*613_*617del
NM_001382769.1:c.*398_*402del	NP_001369698.1:n.*398_*402del
NM_001382770.1:c.*398_*402del	NP_001369699.1:n.*398_*402del
NM_001382771.1:c.*398_*402del	NP_001369700.1:n.*398_*402del
NM_001382772.1:c.*398_*402del	NP_001369701.1:n.*398_*402del
NM_001382773.1:c.*613_*617del	NP_001369702.1:n.*613_*617del
NM_001382774.1:c.*398_*402del	NP_001369703.1:n.*398_*402del