Canonical Allele Identifier: CA420974974

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154420620T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448144T>C , CM000663.2:g.154448144T>C	GRCh38
NC_000001.10:g.154420620T>C , CM000663.1:g.154420620T>C	GRCh37
NC_000001.9:g.152687244T>C	NCBI36
NG_012087.1:g.47952T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.969T>C MANE Select	ENSP00000357470.3:p.Ala323=
ENST00000344086.8:c.969T>C	ENSP00000340589.4:p.Ala323=
ENST00000368485.7:c.969T>C	ENSP00000357470.3:p.Ala323=
ENST00000476006.5:c.785T>C
ENST00000507256.1:n.167T>C
ENST00000515190.1:c.377T>C
NM_000565.3:c.969T>C	NP_000556.1:p.Ala323=
NM_181359.2:c.969T>C	NP_852004.1:p.Ala323=
XM_005245139.1:c.827T>C	XP_005245196.1:p.Leu276Pro
XM_005245140.1:c.827T>C	XP_005245197.1:p.Leu276Pro
XM_006711298.1:c.1017T>C	XP_006711361.1:p.Ala339=
XM_006711299.2:c.1017T>C	XP_006711362.1:p.Ala339=
XM_005245139.2:c.827T>C	XP_005245196.1:p.Leu276Pro
XM_005245140.3:c.827T>C	XP_005245197.1:p.Leu276Pro
XM_006711298.2:c.1017T>C	XP_006711361.1:p.Ala339=
XM_006711299.4:c.1017T>C	XP_006711362.1:p.Ala339=
XM_017001199.2:c.1017T>C	XP_016856688.1:p.Ala339=
XM_017001200.2:c.969T>C	XP_016856689.1:p.Ala323=
XM_017001201.2:c.827T>C	XP_016856690.1:p.Leu276Pro
NM_000565.4:c.969T>C MANE Select	NP_000556.1:p.Ala323=
NM_181359.3:c.969T>C	NP_852004.1:p.Ala323=
NM_001382769.1:c.969T>C	NP_001369698.1:p.Ala323=
NM_001382770.1:c.1062T>C	NP_001369699.1:p.Ala354=
NM_001382771.1:c.1017T>C	NP_001369700.1:p.Ala339=
NM_001382772.1:c.963T>C	NP_001369701.1:p.Ala321=
NM_001382773.1:c.1017T>C	NP_001369702.1:p.Ala339=
NM_001382774.1:c.609T>C	NP_001369703.1:p.Ala203=