Canonical Allele Identifier: CA573293233
Gene: STEAP1B HGNC NCBI
IL6 HGNC NCBI
IL6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1304740438
gnomAD v2: 7-22766481-G-T
gnomAD v3: 7-22726862-G-T
gnomAD v4: 7-22726862-G-T
MyVariant Identifiers: chr7:g.22766481G>T (hg19) chr7:g.22726862G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726862G>T , CM000669.2:g.22726862G>T GRCh38
NC_000007.13:g.22766481G>T , CM000669.1:g.22766481G>T GRCh37
NC_000007.12:g.22733006G>T NCBI36
NG_011640.1:g.4716G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+706C>A (STEAP1B)
ENST00000404625.5:c.-84-317G>T (IL6) ENSP00000385675.1:n.-84-317G>T
NR_131935.1:n.54-157C>A (IL6-AS1)
XM_011515390.1:c.-84-317G>T (IL6) XP_011513692.1:n.-84-317G>T
XM_011515390.2:c.-84-317G>T (IL6) XP_011513692.1:n.-84-317G>T
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