Canonical Allele Identifier: CA342628525

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154437707C>G (hg19) ; chr1:g.154465231C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465231C>G , CM000663.2:g.154465231C>G	GRCh38
NC_000001.10:g.154437707C>G , CM000663.1:g.154437707C>G	GRCh37
NC_000001.9:g.152704331C>G	NCBI36
NG_012087.1:g.65039C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.1258C>G MANE Select	ENSP00000357470.3:p.Pro420Ala
ENST00000344086.8:c.*66C>G	ENSP00000340589.4:n.*66C>G
ENST00000368485.7:c.1258C>G	ENSP00000357470.3:p.Pro420Ala
ENST00000502679.1:n.571C>G
ENST00000507256.1:n.456C>G
NM_000565.3:c.1258C>G	NP_000556.1:p.Pro420Ala
NM_181359.2:c.*66C>G	NP_852004.1:n.*66C>G
XM_005245139.1:c.1022C>G	XP_005245196.1:p.Thr341Ser
XM_005245140.1:c.*99C>G	XP_005245197.1:n.*99C>G
XM_006711298.1:c.1306C>G	XP_006711361.1:p.Pro436Ala
XM_006711299.2:c.*66C>G	XP_006711362.1:n.*66C>G
XM_005245139.2:c.1022C>G	XP_005245196.1:p.Thr341Ser
XM_005245140.3:c.*99C>G	XP_005245197.1:n.*99C>G
XM_006711298.2:c.1306C>G	XP_006711361.1:p.Pro436Ala
XM_006711299.4:c.*66C>G	XP_006711362.1:n.*66C>G
XM_017001199.2:c.1405C>G	XP_016856688.1:p.Pro469Ala
XM_017001200.2:c.1357C>G	XP_016856689.1:p.Pro453Ala
XM_017001201.2:c.*99C>G	XP_016856690.1:n.*99C>G
NM_000565.4:c.1258C>G MANE Select	NP_000556.1:p.Pro420Ala
NM_181359.3:c.*66C>G	NP_852004.1:n.*66C>G
NM_001382769.1:c.1357C>G	NP_001369698.1:p.Pro453Ala
NM_001382770.1:c.1351C>G	NP_001369699.1:p.Pro451Ala
NM_001382771.1:c.1306C>G	NP_001369700.1:p.Pro436Ala
NM_001382772.1:c.1252C>G	NP_001369701.1:p.Pro418Ala
NM_001382773.1:c.*66C>G	NP_001369702.1:n.*66C>G
NM_001382774.1:c.898C>G	NP_001369703.1:p.Pro300Ala