Canonical Allele Identifier: CA420974941
Gene: IL6R HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154420602A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154448126A>G , CM000663.2:g.154448126A>G GRCh38
NC_000001.10:g.154420602A>G , CM000663.1:g.154420602A>G GRCh37
NC_000001.9:g.152687226A>G NCBI36
NG_012087.1:g.47934A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.951A>G MANE Select ENSP00000357470.3:p.Glu317=
ENST00000344086.8:c.951A>G ENSP00000340589.4:p.Glu317=
ENST00000368485.7:c.951A>G ENSP00000357470.3:p.Glu317=
ENST00000476006.5:c.767A>G
ENST00000507256.1:n.149A>G
ENST00000515190.1:c.359A>G
NM_000565.3:c.951A>G NP_000556.1:p.Glu317=
NM_181359.2:c.951A>G NP_852004.1:p.Glu317=
XM_005245139.1:c.809A>G XP_005245196.1:p.Asn270Ser
XM_005245140.1:c.809A>G XP_005245197.1:p.Asn270Ser
XM_006711298.1:c.999A>G XP_006711361.1:p.Glu333=
XM_006711299.2:c.999A>G XP_006711362.1:p.Glu333=
XM_005245139.2:c.809A>G XP_005245196.1:p.Asn270Ser
XM_005245140.3:c.809A>G XP_005245197.1:p.Asn270Ser
XM_006711298.2:c.999A>G XP_006711361.1:p.Glu333=
XM_006711299.4:c.999A>G XP_006711362.1:p.Glu333=
XM_017001199.2:c.999A>G XP_016856688.1:p.Glu333=
XM_017001200.2:c.951A>G XP_016856689.1:p.Glu317=
XM_017001201.2:c.809A>G XP_016856690.1:p.Asn270Ser
NM_000565.4:c.951A>G MANE Select NP_000556.1:p.Glu317=
NM_181359.3:c.951A>G NP_852004.1:p.Glu317=
NM_001382769.1:c.951A>G NP_001369698.1:p.Glu317=
NM_001382770.1:c.1044A>G NP_001369699.1:p.Glu348=
NM_001382771.1:c.999A>G NP_001369700.1:p.Glu333=
NM_001382772.1:c.945A>G NP_001369701.1:p.Glu315=
NM_001382773.1:c.999A>G NP_001369702.1:p.Glu333=
NM_001382774.1:c.591A>G NP_001369703.1:p.Glu197=