Canonical Allele Identifier: CA342621697

Gene: IL6R

Linked Data

• MyVariant Identifiers: chr1:g.154420615C>T (hg19) ; chr1:g.154448139C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154448139C>T , CM000663.2:g.154448139C>T	GRCh38
NC_000001.10:g.154420615C>T , CM000663.1:g.154420615C>T	GRCh37
NC_000001.9:g.152687239C>T	NCBI36
NG_012087.1:g.47947C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.964C>T MANE Select	ENSP00000357470.3:p.Pro322Ser
ENST00000344086.8:c.964C>T	ENSP00000340589.4:p.Pro322Ser
ENST00000368485.7:c.964C>T	ENSP00000357470.3:p.Pro322Ser
ENST00000476006.5:c.780C>T
ENST00000507256.1:n.162C>T
ENST00000515190.1:c.372C>T
NM_000565.3:c.964C>T	NP_000556.1:p.Pro322Ser
NM_181359.2:c.964C>T	NP_852004.1:p.Pro322Ser
XM_005245139.1:c.822C>T	XP_005245196.1:p.Leu274=
XM_005245140.1:c.822C>T	XP_005245197.1:p.Leu274=
XM_006711298.1:c.1012C>T	XP_006711361.1:p.Pro338Ser
XM_006711299.2:c.1012C>T	XP_006711362.1:p.Pro338Ser
XM_005245139.2:c.822C>T	XP_005245196.1:p.Leu274=
XM_005245140.3:c.822C>T	XP_005245197.1:p.Leu274=
XM_006711298.2:c.1012C>T	XP_006711361.1:p.Pro338Ser
XM_006711299.4:c.1012C>T	XP_006711362.1:p.Pro338Ser
XM_017001199.2:c.1012C>T	XP_016856688.1:p.Pro338Ser
XM_017001200.2:c.964C>T	XP_016856689.1:p.Pro322Ser
XM_017001201.2:c.822C>T	XP_016856690.1:p.Leu274=
NM_000565.4:c.964C>T MANE Select	NP_000556.1:p.Pro322Ser
NM_181359.3:c.964C>T	NP_852004.1:p.Pro322Ser
NM_001382769.1:c.964C>T	NP_001369698.1:p.Pro322Ser
NM_001382770.1:c.1057C>T	NP_001369699.1:p.Pro353Ser
NM_001382771.1:c.1012C>T	NP_001369700.1:p.Pro338Ser
NM_001382772.1:c.958C>T	NP_001369701.1:p.Pro320Ser
NM_001382773.1:c.1012C>T	NP_001369702.1:p.Pro338Ser
NM_001382774.1:c.604C>T	NP_001369703.1:p.Pro202Ser