Canonical Allele Identifier: CA2774703257

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726633del , CM000669.2:g.22726633del GRCh38
NC_000007.13:g.22766252del , CM000669.1:g.22766252del GRCh37
NC_000007.12:g.22732777del NCBI36
NG_011640.1:g.4487del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+935del (STEAP1B)
ENST00000404625.5:c.-85+375del (IL6) ENSP00000385675.1:n.-85+375del
NR_131935.1:n.126del (IL6-AS1)
XM_011515390.1:c.-85+375del (IL6) XP_011513692.1:n.-85+375del
XM_011515390.2:c.-85+375del (IL6) XP_011513692.1:n.-85+375del