Canonical Allele Identifier: CA1694138181

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727000C= , CM000669.2:g.22727000C= GRCh38
NC_000007.13:g.22766619C= , CM000669.1:g.22766619C= GRCh37
NC_000007.12:g.22733144C= NCBI36
NG_011640.1:g.4854C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+568G= (STEAP1B)
ENST00000404625.5:c.-84-179C= (IL6) ENSP00000385675.1:n.-84-179C=
NR_131935.1:n.54-295G= (IL6-AS1)
XM_011515390.1:c.-84-179C= (IL6) XP_011513692.1:n.-84-179C=
XM_011515390.2:c.-84-179C= (IL6) XP_011513692.1:n.-84-179C=