Canonical Allele Identifier: CA1694138184

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727001_22727006delinsACTTTT , CM000669.2:g.22727001_22727006delinsACTTTT GRCh38
NC_000007.13:g.22766620_22766625delinsACTTTT , CM000669.1:g.22766620_22766625delinsACTTTT GRCh37
NC_000007.12:g.22733145_22733150delinsACTTTT NCBI36
NG_011640.1:g.4855_4860delinsACTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+562_46+567delinsAAAAGT (STEAP1B)
ENST00000404625.5:c.-84-178_-84-173delinsACTTTT (IL6) ENSP00000385675.1:n.-84-178_-84-173delinsACTTTT
NR_131935.1:n.54-301_54-296delinsAAAAGT (IL6-AS1)
XM_011515390.1:c.-84-178_-84-173delinsACTTTT (IL6) XP_011513692.1:n.-84-178_-84-173delinsACTTTT
XM_011515390.2:c.-84-178_-84-173delinsACTTTT (IL6) XP_011513692.1:n.-84-178_-84-173delinsACTTTT