Canonical Allele Identifier: CA2648156923

Gene: IL6R

Linked Data

• gnomAD v4: 1-154465549-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154465549C>T , CM000663.2:g.154465549C>T	GRCh38
NC_000001.10:g.154438025C>T , CM000663.1:g.154438025C>T	GRCh37
NC_000001.9:g.152704649C>T	NCBI36
NG_012087.1:g.65357C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368485.8:c.*169C>T MANE Select	ENSP00000357470.3:n.*169C>T
ENST00000344086.8:c.*384C>T	ENSP00000340589.4:n.*384C>T
ENST00000368485.7:c.*169C>T	ENSP00000357470.3:n.*169C>T
NM_000565.3:c.*169C>T	NP_000556.1:n.*169C>T
NM_181359.2:c.*384C>T	NP_852004.1:n.*384C>T
XM_005245139.1:c.*257C>T	XP_005245196.1:n.*257C>T
XM_005245140.1:c.*417C>T	XP_005245197.1:n.*417C>T
XM_006711298.1:c.*169C>T	XP_006711361.1:n.*169C>T
XM_005245139.2:c.*257C>T	XP_005245196.1:n.*257C>T
XM_005245140.3:c.*417C>T	XP_005245197.1:n.*417C>T
XM_006711298.2:c.*169C>T	XP_006711361.1:n.*169C>T
XM_017001199.2:c.*169C>T	XP_016856688.1:n.*169C>T
XM_017001200.2:c.*169C>T	XP_016856689.1:n.*169C>T
XM_017001201.2:c.*417C>T	XP_016856690.1:n.*417C>T
NM_000565.4:c.*169C>T MANE Select	NP_000556.1:n.*169C>T
NM_181359.3:c.*384C>T	NP_852004.1:n.*384C>T
NM_001382769.1:c.*169C>T	NP_001369698.1:n.*169C>T
NM_001382770.1:c.*169C>T	NP_001369699.1:n.*169C>T
NM_001382771.1:c.*169C>T	NP_001369700.1:n.*169C>T
NM_001382772.1:c.*169C>T	NP_001369701.1:n.*169C>T
NM_001382773.1:c.*384C>T	NP_001369702.1:n.*384C>T
NM_001382774.1:c.*169C>T	NP_001369703.1:n.*169C>T