Canonical Allele Identifier: CA1694138136

Linked Data

dbSNP Id: rs1784015357

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726919_22726920del , CM000669.2:g.22726919_22726920del GRCh38
NC_000007.13:g.22766538_22766539del , CM000669.1:g.22766538_22766539del GRCh37
NC_000007.12:g.22733063_22733064del NCBI36
NG_011640.1:g.4773_4774del

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+649_46+650del (STEAP1B)
ENST00000404625.5:c.-84-260_-84-259del (IL6) ENSP00000385675.1:n.-84-260_-84-259del
NR_131935.1:n.54-214_54-213del (IL6-AS1)
XM_011515390.1:c.-84-260_-84-259del (IL6) XP_011513692.1:n.-84-260_-84-259del
XM_011515390.2:c.-84-260_-84-259del (IL6) XP_011513692.1:n.-84-260_-84-259del