Canonical Allele Identifier: CA573293222
Gene: STEAP1B HGNC NCBI
IL6 HGNC NCBI
IL6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1424688533
gnomAD v2: 7-22766400-T-C
gnomAD v3: 7-22726781-T-C
gnomAD v4: 7-22726781-T-C
MyVariant Identifiers: chr7:g.22766400T>C (hg19) chr7:g.22726781T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726781T>C , CM000669.2:g.22726781T>C GRCh38
NC_000007.13:g.22766400T>C , CM000669.1:g.22766400T>C GRCh37
NC_000007.12:g.22732925T>C NCBI36
NG_011640.1:g.4635T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+787A>G (STEAP1B)
ENST00000404625.5:c.-84-398T>C (IL6) ENSP00000385675.1:n.-84-398T>C
NR_131935.1:n.54-76A>G (IL6-AS1)
XM_011515390.1:c.-84-398T>C (IL6) XP_011513692.1:n.-84-398T>C
XM_011515390.2:c.-84-398T>C (IL6) XP_011513692.1:n.-84-398T>C
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