Canonical Allele Identifier: CA573293227
Gene: STEAP1B HGNC NCBI
IL6 HGNC NCBI
IL6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1562644623
gnomAD v2: 7-22766434-T-TAAA
gnomAD v3: 7-22726815-T-TAAA
gnomAD v4: 7-22726815-T-TAAA
MyVariant Identifiers: chr7:g.22766434_22766435insAAA (hg19) chr7:g.22726815_22726816insAAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726815_22726816insAAA , CM000669.2:g.22726815_22726816insAAA GRCh38
NC_000007.13:g.22766434_22766435insAAA , CM000669.1:g.22766434_22766435insAAA GRCh37
NC_000007.12:g.22732959_22732960insAAA NCBI36
NG_011640.1:g.4669_4670insAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+752_46+753insTTT (STEAP1B)
ENST00000404625.5:c.-84-364_-84-363insAAA (IL6) ENSP00000385675.1:n.-84-364_-84-363insAAA
NR_131935.1:n.54-111_54-110insTTT (IL6-AS1)
XM_011515390.1:c.-84-364_-84-363insAAA (IL6) XP_011513692.1:n.-84-364_-84-363insAAA
XM_011515390.2:c.-84-364_-84-363insAAA (IL6) XP_011513692.1:n.-84-364_-84-363insAAA
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