Canonical Allele Identifier: CA1694138156

Linked Data

dbSNP Id: rs1784016315

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726945G>A , CM000669.2:g.22726945G>A GRCh38
NC_000007.13:g.22766564G>A , CM000669.1:g.22766564G>A GRCh37
NC_000007.12:g.22733089G>A NCBI36
NG_011640.1:g.4799G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+623C>T (STEAP1B)
ENST00000404625.5:c.-84-234G>A (IL6) ENSP00000385675.1:n.-84-234G>A
NR_131935.1:n.54-240C>T (IL6-AS1)
XM_011515390.1:c.-84-234G>A (IL6) XP_011513692.1:n.-84-234G>A
XM_011515390.2:c.-84-234G>A (IL6) XP_011513692.1:n.-84-234G>A