Canonical Allele Identifier: CA155237904
Gene: STEAP1B HGNC NCBI
IL6 HGNC NCBI
IL6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs192273987
gnomAD v3: 7-22726646-A-G
gnomAD v4: 7-22726646-A-G
MyVariant Identifiers: chr7:g.22766265A>G (hg19) chr7:g.22726646A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726646A>G , CM000669.2:g.22726646A>G GRCh38
NC_000007.13:g.22766265A>G , CM000669.1:g.22766265A>G GRCh37
NC_000007.12:g.22732790A>G NCBI36
NG_011640.1:g.4500A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+922T>C (STEAP1B)
ENST00000404625.5:c.-85+388A>G (IL6) ENSP00000385675.1:n.-85+388A>G
NR_131935.1:n.113T>C (IL6-AS1)
XM_011515390.1:c.-85+388A>G (IL6) XP_011513692.1:n.-85+388A>G
XM_011515390.2:c.-85+388A>G (IL6) XP_011513692.1:n.-85+388A>G
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