Canonical Allele Identifier: CA12500163
Gene: IL6 HGNC NCBI

Linked Data

dbSNP Id: rs1800795

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727026C>G , CM000669.2:g.22727026C>G GRCh38
NC_000007.13:g.22766645C>G , CM000669.1:g.22766645C>G GRCh37
NC_000007.12:g.22733170C>G NCBI36
NG_011640.1:g.4880C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+542G>C
ENST00000404625.5:c.-84-153C>G ENSP00000385675.1:p.=
NR_131935.1:n.54-321G>C
XM_011515390.1:c.-84-153C>G XP_011513692.1:p.=
XM_011515390.2:c.-84-153C>G XP_011513692.1:p.=