Canonical Allele Identifier: CA1099320645

Linked Data

dbSNP Id: rs1784017878

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727003_22727007del , CM000669.2:g.22727003_22727007del GRCh38
NC_000007.13:g.22766622_22766626del , CM000669.1:g.22766622_22766626del GRCh37
NC_000007.12:g.22733147_22733151del NCBI36
NG_011640.1:g.4857_4861del

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+562_46+566del (STEAP1B)
ENST00000404625.5:c.-84-176_-84-172del (IL6) ENSP00000385675.1:n.-84-176_-84-172del
NR_131935.1:n.54-301_54-297del (IL6-AS1)
XM_011515390.1:c.-84-176_-84-172del (IL6) XP_011513692.1:n.-84-176_-84-172del
XM_011515390.2:c.-84-176_-84-172del (IL6) XP_011513692.1:n.-84-176_-84-172del