Canonical Allele Identifier: CA155238306

Linked Data

dbSNP Id: rs780331719

Genomic Alleles

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

Transcript Alleles

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