Canonical Allele Identifier: CA2480880462

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465686C= , CM000663.2:g.154465686C=	GRCh38
NC_000001.10:g.154438162C= , CM000663.1:g.154438162C=	GRCh37
NC_000001.9:g.152704786C=	NCBI36
NG_012087.1:g.65494C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*306C= MANE Select	ENSP00000357470.3:n.*306C=
ENST00000344086.8:c.*521C=	ENSP00000340589.4:n.*521C=
ENST00000368485.7:c.*306C=	ENSP00000357470.3:n.*306C=
NM_000565.3:c.*306C=	NP_000556.1:n.*306C=
NM_181359.2:c.*521C=	NP_852004.1:n.*521C=
XM_005245139.1:c.*394C=	XP_005245196.1:n.*394C=
XM_005245140.1:c.*554C=	XP_005245197.1:n.*554C=
XM_006711298.1:c.*306C=	XP_006711361.1:n.*306C=
XM_005245139.2:c.*394C=	XP_005245196.1:n.*394C=
XM_005245140.3:c.*554C=	XP_005245197.1:n.*554C=
XM_006711298.2:c.*306C=	XP_006711361.1:n.*306C=
XM_017001199.2:c.*306C=	XP_016856688.1:n.*306C=
XM_017001200.2:c.*306C=	XP_016856689.1:n.*306C=
XM_017001201.2:c.*554C=	XP_016856690.1:n.*554C=
NM_000565.4:c.*306C= MANE Select	NP_000556.1:n.*306C=
NM_181359.3:c.*521C=	NP_852004.1:n.*521C=
NM_001382769.1:c.*306C=	NP_001369698.1:n.*306C=
NM_001382770.1:c.*306C=	NP_001369699.1:n.*306C=
NM_001382771.1:c.*306C=	NP_001369700.1:n.*306C=
NM_001382772.1:c.*306C=	NP_001369701.1:n.*306C=
NM_001382773.1:c.*521C=	NP_001369702.1:n.*521C=
NM_001382774.1:c.*306C=	NP_001369703.1:n.*306C=