Canonical Allele Identifier: CA1694138185

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727002_22727003delinsCT , CM000669.2:g.22727002_22727003delinsCT GRCh38
NC_000007.13:g.22766621_22766622delinsCT , CM000669.1:g.22766621_22766622delinsCT GRCh37
NC_000007.12:g.22733146_22733147delinsCT NCBI36
NG_011640.1:g.4856_4857delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+565_46+566delinsAG (STEAP1B)
ENST00000404625.5:c.-84-177_-84-176delinsCT (IL6) ENSP00000385675.1:n.-84-177_-84-176delins...
NR_131935.1:n.54-298_54-297delinsAG (IL6-AS1)
XM_011515390.1:c.-84-177_-84-176delinsCT (IL6) XP_011513692.1:n.-84-177_-84-176delinsCT
XM_011515390.2:c.-84-177_-84-176delinsCT (IL6) XP_011513692.1:n.-84-177_-84-176delinsCT