Canonical Allele Identifier: CA2682013019

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726825_22726826del , CM000669.2:g.22726825_22726826del GRCh38
NC_000007.13:g.22766444_22766445del , CM000669.1:g.22766444_22766445del GRCh37
NC_000007.12:g.22732969_22732970del NCBI36
NG_011640.1:g.4679_4680del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+742_46+743del (STEAP1B)
ENST00000404625.5:c.-84-354_-84-353del (IL6) ENSP00000385675.1:n.-84-354_-84-353del
NR_131935.1:n.54-121_54-120del (IL6-AS1)
XM_011515390.1:c.-84-354_-84-353del (IL6) XP_011513692.1:n.-84-354_-84-353del
XM_011515390.2:c.-84-354_-84-353del (IL6) XP_011513692.1:n.-84-354_-84-353del