Canonical Allele Identifier: CA1694138239

Linked Data

dbSNP Id: rs1784019589
gnomAD v4: 7-22727119-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727119T>A , CM000669.2:g.22727119T>A GRCh38
NC_000007.13:g.22766738T>A , CM000669.1:g.22766738T>A GRCh37
NC_000007.12:g.22733263T>A NCBI36
NG_011640.1:g.4973T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+449A>T (STEAP1B)
ENST00000404625.5:c.-84-60T>A (IL6) ENSP00000385675.1:n.-84-60T>A
NR_131935.1:n.54-414A>T (IL6-AS1)
XM_005249745.3:c.-144T>A (IL6) XP_005249802.1:n.-144T>A
XM_011515390.1:c.-84-60T>A (IL6) XP_011513692.1:n.-84-60T>A
XM_011515390.2:c.-84-60T>A (IL6) XP_011513692.1:n.-84-60T>A