Canonical Allele Identifier: CA2682012876

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726522_22726527del , CM000669.2:g.22726522_22726527del GRCh38
NC_000007.13:g.22766141_22766146del , CM000669.1:g.22766141_22766146del GRCh37
NC_000007.12:g.22732666_22732671del NCBI36
NG_011640.1:g.4376_4381del

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+1043_46+1048del (STEAP1B)
ENST00000404625.5:c.-85+264_-85+269del (IL6) ENSP00000385675.1:n.-85+264_-85+269del
NR_131935.1:n.234_239del (IL6-AS1)
XM_011515390.1:c.-85+264_-85+269del (IL6) XP_011513692.1:n.-85+264_-85+269del
XM_011515390.2:c.-85+264_-85+269del (IL6) XP_011513692.1:n.-85+264_-85+269del