Canonical Allele Identifier: CA1694138220

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727082C= , CM000669.2:g.22727082C= GRCh38
NC_000007.13:g.22766701C= , CM000669.1:g.22766701C= GRCh37
NC_000007.12:g.22733226C= NCBI36
NG_011640.1:g.4936C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+486G= (STEAP1B)
ENST00000404625.5:c.-84-97C= (IL6) ENSP00000385675.1:n.-84-97C=
NR_131935.1:n.54-377G= (IL6-AS1)
XM_005249745.3:c.-181C= (IL6) XP_005249802.1:n.-181C=
XM_011515390.1:c.-84-97C= (IL6) XP_011513692.1:n.-84-97C=
XM_011515390.2:c.-84-97C= (IL6) XP_011513692.1:n.-84-97C=