Canonical Allele Identifier: CA1694138194

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727011_22727012delinsCT , CM000669.2:g.22727011_22727012delinsCT GRCh38
NC_000007.13:g.22766630_22766631delinsCT , CM000669.1:g.22766630_22766631delinsCT GRCh37
NC_000007.12:g.22733155_22733156delinsCT NCBI36
NG_011640.1:g.4865_4866delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+556_46+557delinsAG (STEAP1B)
ENST00000404625.5:c.-84-168_-84-167delinsCT (IL6) ENSP00000385675.1:n.-84-168_-84-167delins...
NR_131935.1:n.54-307_54-306delinsAG (IL6-AS1)
XM_011515390.1:c.-84-168_-84-167delinsCT (IL6) XP_011513692.1:n.-84-168_-84-167delinsCT
XM_011515390.2:c.-84-168_-84-167delinsCT (IL6) XP_011513692.1:n.-84-168_-84-167delinsCT