Canonical Allele Identifier: CA1694138101

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726854_22726856delinsTTC , CM000669.2:g.22726854_22726856delinsTTC GRCh38
NC_000007.13:g.22766473_22766475delinsTTC , CM000669.1:g.22766473_22766475delinsTTC GRCh37
NC_000007.12:g.22732998_22733000delinsTTC NCBI36
NG_011640.1:g.4708_4710delinsTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+712_46+714delinsGAA (STEAP1B)
ENST00000404625.5:c.-84-325_-84-323delinsTTC (IL6) ENSP00000385675.1:n.-84-325_-84-323delinsTTC
NR_131935.1:n.54-151_54-149delinsGAA (IL6-AS1)
XM_011515390.1:c.-84-325_-84-323delinsTTC (IL6) XP_011513692.1:n.-84-325_-84-323delinsTTC
XM_011515390.2:c.-84-325_-84-323delinsTTC (IL6) XP_011513692.1:n.-84-325_-84-323delinsTTC