Canonical Allele Identifier: CA1694137961

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726542C= , CM000669.2:g.22726542C= GRCh38
NC_000007.13:g.22766161C= , CM000669.1:g.22766161C= GRCh37
NC_000007.12:g.22732686C= NCBI36
NG_011640.1:g.4396C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+1026G= (STEAP1B)
ENST00000404625.5:c.-85+284C= (IL6) ENSP00000385675.1:n.-85+284C=
NR_131935.1:n.217G= (IL6-AS1)
XM_011515390.1:c.-85+284C= (IL6) XP_011513692.1:n.-85+284C=
XM_011515390.2:c.-85+284C= (IL6) XP_011513692.1:n.-85+284C=