Canonical Allele Identifier: CA573293231
Gene: STEAP1B HGNC NCBI
IL6 HGNC NCBI
IL6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1370241087
gnomAD v2: 7-22766475-C-T
gnomAD v3: 7-22726856-C-T
gnomAD v4: 7-22726856-C-T
MyVariant Identifiers: chr7:g.22766475C>T (hg19) chr7:g.22726856C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726856C>T , CM000669.2:g.22726856C>T GRCh38
NC_000007.13:g.22766475C>T , CM000669.1:g.22766475C>T GRCh37
NC_000007.12:g.22733000C>T NCBI36
NG_011640.1:g.4710C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+712G>A (STEAP1B)
ENST00000404625.5:c.-84-323C>T (IL6) ENSP00000385675.1:n.-84-323C>T
NR_131935.1:n.54-151G>A (IL6-AS1)
XM_011515390.1:c.-84-323C>T (IL6) XP_011513692.1:n.-84-323C>T
XM_011515390.2:c.-84-323C>T (IL6) XP_011513692.1:n.-84-323C>T
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