Canonical Allele Identifier: CA2682013285

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727100_22727105del , CM000669.2:g.22727100_22727105del GRCh38
NC_000007.13:g.22766719_22766724del , CM000669.1:g.22766719_22766724del GRCh37
NC_000007.12:g.22733244_22733249del NCBI36
NG_011640.1:g.4954_4959del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+470_46+475del (STEAP1B)
ENST00000404625.5:c.-84-79_-84-74del (IL6) ENSP00000385675.1:n.-84-79_-84-74del
NR_131935.1:n.54-393_54-388del (IL6-AS1)
XM_005249745.3:c.-163_-158del (IL6) XP_005249802.1:n.-163_-158del
XM_011515390.1:c.-84-79_-84-74del (IL6) XP_011513692.1:n.-84-79_-84-74del
XM_011515390.2:c.-84-79_-84-74del (IL6) XP_011513692.1:n.-84-79_-84-74del