Canonical Allele Identifier: CA2682012972

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726811_22726813dup , CM000669.2:g.22726811_22726813dup GRCh38
NC_000007.13:g.22766430_22766432dup , CM000669.1:g.22766430_22766432dup GRCh37
NC_000007.12:g.22732955_22732957dup NCBI36
NG_011640.1:g.4665_4667dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+760_46+762dup (STEAP1B)
ENST00000404625.5:c.-84-368_-84-366dup (IL6) ENSP00000385675.1:n.-84-368_-84-366dup
NR_131935.1:n.54-103_54-101dup (IL6-AS1)
XM_011515390.1:c.-84-368_-84-366dup (IL6) XP_011513692.1:n.-84-368_-84-366dup
XM_011515390.2:c.-84-368_-84-366dup (IL6) XP_011513692.1:n.-84-368_-84-366dup