Canonical Allele Identifier: CA155238295

Linked Data

dbSNP Id: rs35178191

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727011dup , CM000669.2:g.22727011dup GRCh38
NC_000007.13:g.22766630dup , CM000669.1:g.22766630dup GRCh37
NC_000007.12:g.22733155dup NCBI36
NG_011640.1:g.4865dup

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+561dup (STEAP1B)
ENST00000404625.5:c.-84-168dup (IL6) ENSP00000385675.1:n.-84-168dup
NR_131935.1:n.54-302dup (IL6-AS1)
XM_011515390.1:c.-84-168dup (IL6) XP_011513692.1:n.-84-168dup
XM_011515390.2:c.-84-168dup (IL6) XP_011513692.1:n.-84-168dup