Canonical Allele Identifier: CA1694138150

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726937_22726941delinsAAAAG , CM000669.2:g.22726937_22726941delinsAAAAG GRCh38
NC_000007.13:g.22766556_22766560delinsAAAAG , CM000669.1:g.22766556_22766560delinsAAAAG GRCh37
NC_000007.12:g.22733081_22733085delinsAAAAG NCBI36
NG_011640.1:g.4791_4795delinsAAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+627_46+631delinsCTTTT (STEAP1B)
ENST00000404625.5:c.-84-242_-84-238delinsAAAAG (IL6) ENSP00000385675.1:n.-84-242_-84-238delinsAAAAG
NR_131935.1:n.54-236_54-232delinsCTTTT (IL6-AS1)
XM_011515390.1:c.-84-242_-84-238delinsAAAAG (IL6) XP_011513692.1:n.-84-242_-84-238delinsAAAAG
XM_011515390.2:c.-84-242_-84-238delinsAAAAG (IL6) XP_011513692.1:n.-84-242_-84-238delinsAAAAG