Canonical Allele Identifier: CA2682012879

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726547del , CM000669.2:g.22726547del GRCh38
NC_000007.13:g.22766166del , CM000669.1:g.22766166del GRCh37
NC_000007.12:g.22732691del NCBI36
NG_011640.1:g.4401del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+1025del (STEAP1B)
ENST00000404625.5:c.-85+289del (IL6) ENSP00000385675.1:n.-85+289del
NR_131935.1:n.216del (IL6-AS1)
XM_011515390.1:c.-85+289del (IL6) XP_011513692.1:n.-85+289del
XM_011515390.2:c.-85+289del (IL6) XP_011513692.1:n.-85+289del