Canonical Allele Identifier: CA1694138158

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726952A= , CM000669.2:g.22726952A= GRCh38
NC_000007.13:g.22766571A= , CM000669.1:g.22766571A= GRCh37
NC_000007.12:g.22733096A= NCBI36
NG_011640.1:g.4806A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+616T= (STEAP1B)
ENST00000404625.5:c.-84-227A= (IL6) ENSP00000385675.1:n.-84-227A=
NR_131935.1:n.54-247T= (IL6-AS1)
XM_011515390.1:c.-84-227A= (IL6) XP_011513692.1:n.-84-227A=
XM_011515390.2:c.-84-227A= (IL6) XP_011513692.1:n.-84-227A=