Canonical Allele Identifier: CA453973132
Gene: STEAP1B HGNC NCBI
IL6 HGNC NCBI
IL6-AS1 HGNC NCBI

Linked Data

gnomAD v4: 7-22726443-A-G
MyVariant Identifiers: chr7:g.22766062A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726443A>G , CM000669.2:g.22726443A>G GRCh38
NC_000007.13:g.22766062A>G , CM000669.1:g.22766062A>G GRCh37
NC_000007.12:g.22732587A>G NCBI36
NG_011640.1:g.4297A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+1125T>C (STEAP1B)
ENST00000404625.5:c.-85+185A>G (IL6) ENSP00000385675.1:n.-85+185A>G
NR_131935.1:n.316T>C (IL6-AS1)
XM_011515390.1:c.-85+185A>G (IL6) XP_011513692.1:n.-85+185A>G
XM_011515390.2:c.-85+185A>G (IL6) XP_011513692.1:n.-85+185A>G
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