Canonical Allele Identifier: CA12557771

Linked Data

dbSNP Id: rs7802308
gnomAD v2: 7-22766434-T-A
gnomAD v3: 7-22726815-T-A
gnomAD v4: 7-22726815-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726815T>A , CM000669.2:g.22726815T>A GRCh38
NC_000007.13:g.22766434T>A , CM000669.1:g.22766434T>A GRCh37
NC_000007.12:g.22732959T>A NCBI36
NG_011640.1:g.4669T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+753A>T (STEAP1B)
ENST00000404625.5:c.-84-364T>A (IL6) ENSP00000385675.1:n.-84-364T>A
NR_131935.1:n.54-110A>T (IL6-AS1)
XM_011515390.1:c.-84-364T>A (IL6) XP_011513692.1:n.-84-364T>A
XM_011515390.2:c.-84-364T>A (IL6) XP_011513692.1:n.-84-364T>A