Canonical Allele Identifier: CA836769494

Linked Data

dbSNP Id: rs1339718644
gnomAD v3: 7-22727039-G-A
gnomAD v4: 7-22727039-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727039G>A , CM000669.2:g.22727039G>A GRCh38
NC_000007.13:g.22766658G>A , CM000669.1:g.22766658G>A GRCh37
NC_000007.12:g.22733183G>A NCBI36
NG_011640.1:g.4893G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+529C>T (STEAP1B)
ENST00000404625.5:c.-84-140G>A (IL6) ENSP00000385675.1:n.-84-140G>A
NR_131935.1:n.54-334C>T (IL6-AS1)
XM_011515390.1:c.-84-140G>A (IL6) XP_011513692.1:n.-84-140G>A
XM_011515390.2:c.-84-140G>A (IL6) XP_011513692.1:n.-84-140G>A