Canonical Allele Identifier: CA1694138162

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726967T= , CM000669.2:g.22726967T= GRCh38
NC_000007.13:g.22766586T= , CM000669.1:g.22766586T= GRCh37
NC_000007.12:g.22733111T= NCBI36
NG_011640.1:g.4821T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+601A= (STEAP1B)
ENST00000404625.5:c.-84-212T= (IL6) ENSP00000385675.1:n.-84-212T=
NR_131935.1:n.54-262A= (IL6-AS1)
XM_011515390.1:c.-84-212T= (IL6) XP_011513692.1:n.-84-212T=
XM_011515390.2:c.-84-212T= (IL6) XP_011513692.1:n.-84-212T=