Canonical Allele Identifier: CA1099320664

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727027_22727040del , CM000669.2:g.22727027_22727040del GRCh38
NC_000007.13:g.22766646_22766659del , CM000669.1:g.22766646_22766659del GRCh37
NC_000007.12:g.22733171_22733184del NCBI36
NG_011640.1:g.4881_4894del

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+528_46+541del (STEAP1B)
ENST00000404625.5:c.-84-152_-84-139del (IL6) ENSP00000385675.1:n.-84-152_-84-139del
NR_131935.1:n.54-335_54-322del (IL6-AS1)
XM_011515390.1:c.-84-152_-84-139del (IL6) XP_011513692.1:n.-84-152_-84-139del
XM_011515390.2:c.-84-152_-84-139del (IL6) XP_011513692.1:n.-84-152_-84-139del