Canonical Allele Identifier: CA836769365

Linked Data

dbSNP Id: rs1357562662

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726420_22726428del , CM000669.2:g.22726420_22726428del GRCh38
NC_000007.13:g.22766039_22766047del , CM000669.1:g.22766039_22766047del GRCh37
NC_000007.12:g.22732564_22732572del NCBI36
NG_011640.1:g.4274_4282del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+1143_46+1151del (STEAP1B)
ENST00000404625.5:c.-85+162_-85+170del (IL6) ENSP00000385675.1:n.-85+162_-85+170del
NR_131935.1:n.334_342del (IL6-AS1)
XM_011515390.1:c.-85+162_-85+170del (IL6) XP_011513692.1:n.-85+162_-85+170del
XM_011515390.2:c.-85+162_-85+170del (IL6) XP_011513692.1:n.-85+162_-85+170del