Canonical Allele Identifier: CA420975879

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437667G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465191G>C , CM000663.2:g.154465191G>C	GRCh38
NC_000001.10:g.154437667G>C , CM000663.1:g.154437667G>C	GRCh37
NC_000001.9:g.152704291G>C	NCBI36
NG_012087.1:g.64999G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1218G>C MANE Select	ENSP00000357470.3:p.Pro406=
ENST00000344086.8:c.*26G>C	ENSP00000340589.4:n.*26G>C
ENST00000368485.7:c.1218G>C	ENSP00000357470.3:p.Pro406=
ENST00000502679.1:n.531G>C
ENST00000507256.1:n.416G>C
NM_000565.3:c.1218G>C	NP_000556.1:p.Pro406=
NM_181359.2:c.*26G>C	NP_852004.1:n.*26G>C
XM_005245139.1:c.982G>C	XP_005245196.1:p.Ala328Pro
XM_005245140.1:c.*59G>C	XP_005245197.1:n.*59G>C
XM_006711298.1:c.1266G>C	XP_006711361.1:p.Pro422=
XM_006711299.2:c.*26G>C	XP_006711362.1:n.*26G>C
XM_005245139.2:c.982G>C	XP_005245196.1:p.Ala328Pro
XM_005245140.3:c.*59G>C	XP_005245197.1:n.*59G>C
XM_006711298.2:c.1266G>C	XP_006711361.1:p.Pro422=
XM_006711299.4:c.*26G>C	XP_006711362.1:n.*26G>C
XM_017001199.2:c.1365G>C	XP_016856688.1:p.Pro455=
XM_017001200.2:c.1317G>C	XP_016856689.1:p.Pro439=
XM_017001201.2:c.*59G>C	XP_016856690.1:n.*59G>C
NM_000565.4:c.1218G>C MANE Select	NP_000556.1:p.Pro406=
NM_181359.3:c.*26G>C	NP_852004.1:n.*26G>C
NM_001382769.1:c.1317G>C	NP_001369698.1:p.Pro439=
NM_001382770.1:c.1311G>C	NP_001369699.1:p.Pro437=
NM_001382771.1:c.1266G>C	NP_001369700.1:p.Pro422=
NM_001382772.1:c.1212G>C	NP_001369701.1:p.Pro404=
NM_001382773.1:c.*26G>C	NP_001369702.1:n.*26G>C
NM_001382774.1:c.858G>C	NP_001369703.1:p.Pro286=