Canonical Allele Identifier: CA2682013179

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727031_22727038del , CM000669.2:g.22727031_22727038del GRCh38
NC_000007.13:g.22766650_22766657del , CM000669.1:g.22766650_22766657del GRCh37
NC_000007.12:g.22733175_22733182del NCBI36
NG_011640.1:g.4885_4892del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+531_46+538del (STEAP1B)
ENST00000404625.5:c.-84-148_-84-141del (IL6) ENSP00000385675.1:n.-84-148_-84-141del
NR_131935.1:n.54-332_54-325del (IL6-AS1)
XM_011515390.1:c.-84-148_-84-141del (IL6) XP_011513692.1:n.-84-148_-84-141del
XM_011515390.2:c.-84-148_-84-141del (IL6) XP_011513692.1:n.-84-148_-84-141del