Canonical Allele Identifier: CA836769456
Gene: STEAP1B HGNC NCBI
IL6 HGNC NCBI
IL6-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1314617691
gnomAD v3: 7-22726839-TTTAGC-T
gnomAD v4: 7-22726839-TTTAGC-T
MyVariant Identifiers: chr7:g.22766459_22766463del (hg19) chr7:g.22726840_22726844del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726843_22726847del , CM000669.2:g.22726843_22726847del GRCh38
NC_000007.13:g.22766462_22766466del , CM000669.1:g.22766462_22766466del GRCh37
NC_000007.12:g.22732987_22732991del NCBI36
NG_011640.1:g.4697_4701del

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+724_46+728del (STEAP1B)
ENST00000404625.5:c.-84-336_-84-332del (IL6) ENSP00000385675.1:n.-84-336_-84-332del
NR_131935.1:n.54-139_54-135del (IL6-AS1)
XM_011515390.1:c.-84-336_-84-332del (IL6) XP_011513692.1:n.-84-336_-84-332del
XM_011515390.2:c.-84-336_-84-332del (IL6) XP_011513692.1:n.-84-336_-84-332del
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