Canonical Allele Identifier: CA342621706

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154420616C>T (hg19) ; chr1:g.154448140C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448140C>T , CM000663.2:g.154448140C>T	GRCh38
NC_000001.10:g.154420616C>T , CM000663.1:g.154420616C>T	GRCh37
NC_000001.9:g.152687240C>T	NCBI36
NG_012087.1:g.47948C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368485.8:c.965C>T MANE Select	ENSP00000357470.3:p.Pro322Leu
ENST00000344086.8:c.965C>T	ENSP00000340589.4:p.Pro322Leu
ENST00000368485.7:c.965C>T	ENSP00000357470.3:p.Pro322Leu
ENST00000476006.5:c.781C>T
ENST00000507256.1:n.163C>T
ENST00000515190.1:c.373C>T
NM_000565.3:c.965C>T	NP_000556.1:p.Pro322Leu
NM_181359.2:c.965C>T	NP_852004.1:p.Pro322Leu
XM_005245139.1:c.823C>T	XP_005245196.1:p.Gln275Ter
XM_005245140.1:c.823C>T	XP_005245197.1:p.Gln275Ter
XM_006711298.1:c.1013C>T	XP_006711361.1:p.Pro338Leu
XM_006711299.2:c.1013C>T	XP_006711362.1:p.Pro338Leu
XM_005245139.2:c.823C>T	XP_005245196.1:p.Gln275Ter
XM_005245140.3:c.823C>T	XP_005245197.1:p.Gln275Ter
XM_006711298.2:c.1013C>T	XP_006711361.1:p.Pro338Leu
XM_006711299.4:c.1013C>T	XP_006711362.1:p.Pro338Leu
XM_017001199.2:c.1013C>T	XP_016856688.1:p.Pro338Leu
XM_017001200.2:c.965C>T	XP_016856689.1:p.Pro322Leu
XM_017001201.2:c.823C>T	XP_016856690.1:p.Gln275Ter
NM_000565.4:c.965C>T MANE Select	NP_000556.1:p.Pro322Leu
NM_181359.3:c.965C>T	NP_852004.1:p.Pro322Leu
NM_001382769.1:c.965C>T	NP_001369698.1:p.Pro322Leu
NM_001382770.1:c.1058C>T	NP_001369699.1:p.Pro353Leu
NM_001382771.1:c.1013C>T	NP_001369700.1:p.Pro338Leu
NM_001382772.1:c.959C>T	NP_001369701.1:p.Pro320Leu
NM_001382773.1:c.1013C>T	NP_001369702.1:p.Pro338Leu
NM_001382774.1:c.605C>T	NP_001369703.1:p.Pro202Leu