Canonical Allele Identifier: CA572945406
Gene: STEAP1B HGNC NCBI
IL6 HGNC NCBI
IL6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1241875315
gnomAD v2: 7-22766631-T-A
MyVariant Identifiers: chr7:g.22766631T>A (hg19) chr7:g.22727012T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727012T>A , CM000669.2:g.22727012T>A GRCh38
NC_000007.13:g.22766631T>A , CM000669.1:g.22766631T>A GRCh37
NC_000007.12:g.22733156T>A NCBI36
NG_011640.1:g.4866T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+556A>T (STEAP1B)
ENST00000404625.5:c.-84-167T>A (IL6) ENSP00000385675.1:n.-84-167T>A
NR_131935.1:n.54-307A>T (IL6-AS1)
XM_011515390.1:c.-84-167T>A (IL6) XP_011513692.1:n.-84-167T>A
XM_011515390.2:c.-84-167T>A (IL6) XP_011513692.1:n.-84-167T>A
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