Canonical Allele Identifier: CA1694138195

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727012T= , CM000669.2:g.22727012T= GRCh38
NC_000007.13:g.22766631T= , CM000669.1:g.22766631T= GRCh37
NC_000007.12:g.22733156T= NCBI36
NG_011640.1:g.4866T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+556A= (STEAP1B)
ENST00000404625.5:c.-84-167T= (IL6) ENSP00000385675.1:n.-84-167T=
NR_131935.1:n.54-307A= (IL6-AS1)
XM_011515390.1:c.-84-167T= (IL6) XP_011513692.1:n.-84-167T=
XM_011515390.2:c.-84-167T= (IL6) XP_011513692.1:n.-84-167T=