Canonical Allele Identifier: CA342628677

Gene: IL6R

Linked Data

• dbSNP Id: rs1691502650
• gnomAD v3: 1-154465309-A-T
• gnomAD v4: 1-154465309-A-T
• MyVariant Identifiers: chr1:g.154437785A>T (hg19) ; chr1:g.154465309A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465309A>T , CM000663.2:g.154465309A>T	GRCh38
NC_000001.10:g.154437785A>T , CM000663.1:g.154437785A>T	GRCh37
NC_000001.9:g.152704409A>T	NCBI36
NG_012087.1:g.65117A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1336A>T MANE Select	ENSP00000357470.3:p.Asn446Tyr
ENST00000344086.8:c.*144A>T	ENSP00000340589.4:n.*144A>T
ENST00000368485.7:c.1336A>T	ENSP00000357470.3:p.Asn446Tyr
ENST00000507256.1:n.534A>T
NM_000565.3:c.1336A>T	NP_000556.1:p.Asn446Tyr
NM_181359.2:c.*144A>T	NP_852004.1:n.*144A>T
XM_005245139.1:c.*17A>T	XP_005245196.1:n.*17A>T
XM_005245140.1:c.*177A>T	XP_005245197.1:n.*177A>T
XM_006711298.1:c.1384A>T	XP_006711361.1:p.Asn462Tyr
XM_005245139.2:c.*17A>T	XP_005245196.1:n.*17A>T
XM_005245140.3:c.*177A>T	XP_005245197.1:n.*177A>T
XM_006711298.2:c.1384A>T	XP_006711361.1:p.Asn462Tyr
XM_017001199.2:c.1483A>T	XP_016856688.1:p.Asn495Tyr
XM_017001200.2:c.1435A>T	XP_016856689.1:p.Asn479Tyr
XM_017001201.2:c.*177A>T	XP_016856690.1:n.*177A>T
NM_000565.4:c.1336A>T MANE Select	NP_000556.1:p.Asn446Tyr
NM_181359.3:c.*144A>T	NP_852004.1:n.*144A>T
NM_001382769.1:c.1435A>T	NP_001369698.1:p.Asn479Tyr
NM_001382770.1:c.1429A>T	NP_001369699.1:p.Asn477Tyr
NM_001382771.1:c.1384A>T	NP_001369700.1:p.Asn462Tyr
NM_001382772.1:c.1330A>T	NP_001369701.1:p.Asn444Tyr
NM_001382773.1:c.*144A>T	NP_001369702.1:n.*144A>T
NM_001382774.1:c.976A>T	NP_001369703.1:p.Asn326Tyr