Canonical Allele Identifier: CA1694138232

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727106C= , CM000669.2:g.22727106C= GRCh38
NC_000007.13:g.22766725C= , CM000669.1:g.22766725C= GRCh37
NC_000007.12:g.22733250C= NCBI36
NG_011640.1:g.4960C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+462G= (STEAP1B)
ENST00000404625.5:c.-84-73C= (IL6) ENSP00000385675.1:n.-84-73C=
NR_131935.1:n.54-401G= (IL6-AS1)
XM_005249745.3:c.-157C= (IL6) XP_005249802.1:n.-157C=
XM_011515390.1:c.-84-73C= (IL6) XP_011513692.1:n.-84-73C=
XM_011515390.2:c.-84-73C= (IL6) XP_011513692.1:n.-84-73C=