Canonical Allele Identifier: CA1694138168

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726984A= , CM000669.2:g.22726984A= GRCh38
NC_000007.13:g.22766603A= , CM000669.1:g.22766603A= GRCh37
NC_000007.12:g.22733128A= NCBI36
NG_011640.1:g.4838A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+584T= (STEAP1B)
ENST00000404625.5:c.-84-195A= (IL6) ENSP00000385675.1:n.-84-195A=
NR_131935.1:n.54-279T= (IL6-AS1)
XM_011515390.1:c.-84-195A= (IL6) XP_011513692.1:n.-84-195A=
XM_011515390.2:c.-84-195A= (IL6) XP_011513692.1:n.-84-195A=