Canonical Allele Identifier: CA2480880517
Gene: IL6R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154465813_154465814delinsTG , CM000663.2:g.154465813_154465814delinsTG GRCh38
NC_000001.10:g.154438289_154438290delinsTG , CM000663.1:g.154438289_154438290delinsTG GRCh37
NC_000001.9:g.152704913_152704914delinsTG NCBI36
NG_012087.1:g.65621_65622delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368485.8:c.*433_*434delinsTG MANE Select ENSP00000357470.3:n.*433_*434delinsTG
ENST00000344086.8:c.*648_*649delinsTG ENSP00000340589.4:n.*648_*649delinsTG
ENST00000368485.7:c.*433_*434delinsTG ENSP00000357470.3:n.*433_*434delinsTG
NM_000565.3:c.*433_*434delinsTG NP_000556.1:n.*433_*434delinsTG
NM_181359.2:c.*648_*649delinsTG NP_852004.1:n.*648_*649delinsTG
XM_005245139.1:c.*521_*522delinsTG XP_005245196.1:n.*521_*522delinsTG
XM_005245140.1:c.*681_*682delinsTG XP_005245197.1:n.*681_*682delinsTG
XM_006711298.1:c.*433_*434delinsTG XP_006711361.1:n.*433_*434delinsTG
XM_005245139.2:c.*521_*522delinsTG XP_005245196.1:n.*521_*522delinsTG
XM_005245140.3:c.*681_*682delinsTG XP_005245197.1:n.*681_*682delinsTG
XM_006711298.2:c.*433_*434delinsTG XP_006711361.1:n.*433_*434delinsTG
XM_017001199.2:c.*433_*434delinsTG XP_016856688.1:n.*433_*434delinsTG
XM_017001200.2:c.*433_*434delinsTG XP_016856689.1:n.*433_*434delinsTG
XM_017001201.2:c.*681_*682delinsTG XP_016856690.1:n.*681_*682delinsTG
NM_000565.4:c.*433_*434delinsTG MANE Select NP_000556.1:n.*433_*434delinsTG
NM_181359.3:c.*648_*649delinsTG NP_852004.1:n.*648_*649delinsTG
NM_001382769.1:c.*433_*434delinsTG NP_001369698.1:n.*433_*434delinsTG
NM_001382770.1:c.*433_*434delinsTG NP_001369699.1:n.*433_*434delinsTG
NM_001382771.1:c.*433_*434delinsTG NP_001369700.1:n.*433_*434delinsTG
NM_001382772.1:c.*433_*434delinsTG NP_001369701.1:n.*433_*434delinsTG
NM_001382773.1:c.*648_*649delinsTG NP_001369702.1:n.*648_*649delinsTG
NM_001382774.1:c.*433_*434delinsTG NP_001369703.1:n.*433_*434delinsTG