Canonical Allele Identifier: CA453973419

Linked Data

dbSNP Id: rs1170714794
gnomAD v3: 7-22726542-C-G
gnomAD v4: 7-22726542-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726542C>G , CM000669.2:g.22726542C>G GRCh38
NC_000007.13:g.22766161C>G , CM000669.1:g.22766161C>G GRCh37
NC_000007.12:g.22732686C>G NCBI36
NG_011640.1:g.4396C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+1026G>C (STEAP1B)
ENST00000404625.5:c.-85+284C>G (IL6) ENSP00000385675.1:n.-85+284C>G
NR_131935.1:n.217G>C (IL6-AS1)
XM_011515390.1:c.-85+284C>G (IL6) XP_011513692.1:n.-85+284C>G
XM_011515390.2:c.-85+284C>G (IL6) XP_011513692.1:n.-85+284C>G