Canonical Allele Identifier: CA1694138222

Linked Data

dbSNP Id: rs1784019096

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727084C>T , CM000669.2:g.22727084C>T GRCh38
NC_000007.13:g.22766703C>T , CM000669.1:g.22766703C>T GRCh37
NC_000007.12:g.22733228C>T NCBI36
NG_011640.1:g.4938C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+484G>A (STEAP1B)
ENST00000404625.5:c.-84-95C>T (IL6) ENSP00000385675.1:n.-84-95C>T
NR_131935.1:n.54-379G>A (IL6-AS1)
XM_005249745.3:c.-179C>T (IL6) XP_005249802.1:n.-179C>T
XM_011515390.1:c.-84-95C>T (IL6) XP_011513692.1:n.-84-95C>T
XM_011515390.2:c.-84-95C>T (IL6) XP_011513692.1:n.-84-95C>T