Canonical Allele Identifier: CA1694138205

Linked Data

dbSNP Id: rs1784018686
gnomAD v4: 7-22727027-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727027A>T , CM000669.2:g.22727027A>T GRCh38
NC_000007.13:g.22766646A>T , CM000669.1:g.22766646A>T GRCh37
NC_000007.12:g.22733171A>T NCBI36
NG_011640.1:g.4881A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+541T>A (STEAP1B)
ENST00000404625.5:c.-84-152A>T (IL6) ENSP00000385675.1:n.-84-152A>T
NR_131935.1:n.54-322T>A (IL6-AS1)
XM_011515390.1:c.-84-152A>T (IL6) XP_011513692.1:n.-84-152A>T
XM_011515390.2:c.-84-152A>T (IL6) XP_011513692.1:n.-84-152A>T