Canonical Allele Identifier: CA1694138074

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726813_22726818delinsATTTTT , CM000669.2:g.22726813_22726818delinsATTTTT GRCh38
NC_000007.13:g.22766432_22766437delinsATTTTT , CM000669.1:g.22766432_22766437delinsATTTTT GRCh37
NC_000007.12:g.22732957_22732962delinsATTTTT NCBI36
NG_011640.1:g.4667_4672delinsATTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+750_46+755delinsAAAAAT (STEAP1B)
ENST00000404625.5:c.-84-366_-84-361delinsATTTTT (IL6) ENSP00000385675.1:n.-84-366_-84-361delinsATTTTT
NR_131935.1:n.54-113_54-108delinsAAAAAT (IL6-AS1)
XM_011515390.1:c.-84-366_-84-361delinsATTTTT (IL6) XP_011513692.1:n.-84-366_-84-361delinsATTTTT
XM_011515390.2:c.-84-366_-84-361delinsATTTTT (IL6) XP_011513692.1:n.-84-366_-84-361delinsATTTTT