Canonical Allele Identifier: CA2682013257

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727078del , CM000669.2:g.22727078del GRCh38
NC_000007.13:g.22766697del , CM000669.1:g.22766697del GRCh37
NC_000007.12:g.22733222del NCBI36
NG_011640.1:g.4932del

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+493del (STEAP1B)
ENST00000404625.5:c.-84-101del (IL6) ENSP00000385675.1:n.-84-101del
NR_131935.1:n.54-370del (IL6-AS1)
XM_011515390.1:c.-84-101del (IL6) XP_011513692.1:n.-84-101del
XM_011515390.2:c.-84-101del (IL6) XP_011513692.1:n.-84-101del