Canonical Allele Identifier: CA10971875

Gene: IL6R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154438943A>C , CM000663.2:g.154438943A>C	GRCh38
NC_000001.10:g.154411419A>C , CM000663.1:g.154411419A>C	GRCh37
NC_000001.9:g.152678043A>C	NCBI36
NG_012087.1:g.38751A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000565.4:c.949+2833A>C MANE Select	NP_000556.1:n.949+2833A>C
ENST00000368485.8:c.949+2833A>C MANE Select	ENSP00000357470.3:n.949+2833A>C
NM_000565.3:c.949+2833A>C	NP_000556.1:n.949+2833A>C
NM_001382769.1:c.949+2833A>C	NP_001369698.1:n.949+2833A>C
NM_001382770.1:c.949+2833A>C	NP_001369699.1:n.949+2833A>C
NM_001382771.1:c.949+2833A>C	NP_001369700.1:n.949+2833A>C
NM_001382772.1:c.943+2833A>C	NP_001369701.1:n.943+2833A>C
NM_001382773.1:c.949+2833A>C	NP_001369702.1:n.949+2833A>C
NM_001382774.1:c.589+2833A>C	NP_001369703.1:n.589+2833A>C
NM_181359.2:c.949+2833A>C	NP_852004.1:n.949+2833A>C
NM_181359.3:c.949+2833A>C	NP_852004.1:n.949+2833A>C
ENST00000344086.8:c.949+2833A>C	ENSP00000340589.4:n.949+2833A>C
ENST00000368485.7:c.949+2833A>C	ENSP00000357470.3:n.949+2833A>C
ENST00000476006.5:c.717+2833A>C
ENST00000507256.1:n.147+3787A>C
ENST00000515190.1:c.357+2833A>C
XM_005245139.1:c.807+3787A>C	XP_005245196.1:n.807+3787A>C
XM_005245139.2:c.807+3787A>C	XP_005245196.1:n.807+3787A>C
XM_005245140.1:c.807+3787A>C	XP_005245197.1:n.807+3787A>C
XM_005245140.3:c.807+3787A>C	XP_005245197.1:n.807+3787A>C
XM_006711298.1:c.949+2833A>C	XP_006711361.1:n.949+2833A>C
XM_006711298.2:c.949+2833A>C	XP_006711361.1:n.949+2833A>C
XM_006711299.2:c.949+2833A>C	XP_006711362.1:n.949+2833A>C
XM_006711299.4:c.949+2833A>C	XP_006711362.1:n.949+2833A>C
XM_017001199.2:c.949+2833A>C	XP_016856688.1:n.949+2833A>C
XM_017001200.2:c.949+2833A>C	XP_016856689.1:n.949+2833A>C
XM_017001201.2:c.807+3787A>C	XP_016856690.1:n.807+3787A>C