Canonical Allele Identifier: CA453973397
Gene: STEAP1B HGNC NCBI
IL6 HGNC NCBI
IL6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1327323047
gnomAD v4: 7-22726535-G-A
MyVariant Identifiers: chr7:g.22766154G>A (hg19) chr7:g.22726535G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726535G>A , CM000669.2:g.22726535G>A GRCh38
NC_000007.13:g.22766154G>A , CM000669.1:g.22766154G>A GRCh37
NC_000007.12:g.22732679G>A NCBI36
NG_011640.1:g.4389G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+1033C>T (STEAP1B)
ENST00000404625.5:c.-85+277G>A (IL6) ENSP00000385675.1:n.-85+277G>A
NR_131935.1:n.224C>T (IL6-AS1)
XM_011515390.1:c.-85+277G>A (IL6) XP_011513692.1:n.-85+277G>A
XM_011515390.2:c.-85+277G>A (IL6) XP_011513692.1:n.-85+277G>A
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