Canonical Allele Identifier: CA1694138254

Linked Data

dbSNP Id: rs1784020107

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727167del , CM000669.2:g.22727167del GRCh38
NC_000007.13:g.22766786del , CM000669.1:g.22766786del GRCh37
NC_000007.12:g.22733311del NCBI36
NG_011640.1:g.5021del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+405del (STEAP1B)
ENST00000258743.9:c.-96del (IL6) ENSP00000258743.5:n.-96del
ENST00000401651.5:c.-133del (IL6) ENSP00000385718.1:n.-133del
ENST00000404625.5:c.-84-12del (IL6) ENSP00000385675.1:n.-84-12del
ENST00000426291.5:c.-96del (IL6) ENSP00000405150.1:n.-96del
NM_000600.3:c.-96del (IL6) NP_000591.1:n.-96del
NR_131935.1:n.53+405del (IL6-AS1)
XM_005249745.3:c.-96del (IL6) XP_005249802.1:n.-96del
XM_011515390.1:c.-84-12del (IL6) XP_011513692.1:n.-84-12del
XM_011515391.1:c.-133del (IL6) XP_011513693.1:n.-133del
NM_000600.4:c.-96del (IL6) NP_000591.1:n.-96del
NM_001318095.1:c.-133del (IL6) NP_001305024.1:n.-133del
XM_005249745.5:c.-96del (IL6) XP_005249802.1:n.-96del
XM_011515390.2:c.-84-12del (IL6) XP_011513692.1:n.-84-12del