Canonical Allele Identifier: CA420976042

Gene: IL6R

Linked Data

• gnomAD v4: 1-154465359-A-T
• MyVariant Identifiers: chr1:g.154437835A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465359A>T , CM000663.2:g.154465359A>T	GRCh38
NC_000001.10:g.154437835A>T , CM000663.1:g.154437835A>T	GRCh37
NC_000001.9:g.152704459A>T	NCBI36
NG_012087.1:g.65167A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368485.8:c.1386A>T MANE Select	ENSP00000357470.3:p.Thr462=
ENST00000344086.8:c.*194A>T	ENSP00000340589.4:n.*194A>T
ENST00000368485.7:c.1386A>T	ENSP00000357470.3:p.Thr462=
NM_000565.3:c.1386A>T	NP_000556.1:p.Thr462=
NM_181359.2:c.*194A>T	NP_852004.1:n.*194A>T
XM_005245139.1:c.*67A>T	XP_005245196.1:n.*67A>T
XM_005245140.1:c.*227A>T	XP_005245197.1:n.*227A>T
XM_006711298.1:c.1434A>T	XP_006711361.1:p.Thr478=
XM_005245139.2:c.*67A>T	XP_005245196.1:n.*67A>T
XM_005245140.3:c.*227A>T	XP_005245197.1:n.*227A>T
XM_006711298.2:c.1434A>T	XP_006711361.1:p.Thr478=
XM_017001199.2:c.1533A>T	XP_016856688.1:p.Thr511=
XM_017001200.2:c.1485A>T	XP_016856689.1:p.Thr495=
XM_017001201.2:c.*227A>T	XP_016856690.1:n.*227A>T
NM_000565.4:c.1386A>T MANE Select	NP_000556.1:p.Thr462=
NM_181359.3:c.*194A>T	NP_852004.1:n.*194A>T
NM_001382769.1:c.1485A>T	NP_001369698.1:p.Thr495=
NM_001382770.1:c.1479A>T	NP_001369699.1:p.Thr493=
NM_001382771.1:c.1434A>T	NP_001369700.1:p.Thr478=
NM_001382772.1:c.1380A>T	NP_001369701.1:p.Thr460=
NM_001382773.1:c.*194A>T	NP_001369702.1:n.*194A>T
NM_001382774.1:c.1026A>T	NP_001369703.1:p.Thr342=