Canonical Allele Identifier: CA1694138112

Linked Data

dbSNP Id: rs1784014549

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726867A>C , CM000669.2:g.22726867A>C GRCh38
NC_000007.13:g.22766486A>C , CM000669.1:g.22766486A>C GRCh37
NC_000007.12:g.22733011A>C NCBI36
NG_011640.1:g.4721A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+701T>G (STEAP1B)
ENST00000404625.5:c.-84-312A>C (IL6) ENSP00000385675.1:n.-84-312A>C
NR_131935.1:n.54-162T>G (IL6-AS1)
XM_011515390.1:c.-84-312A>C (IL6) XP_011513692.1:n.-84-312A>C
XM_011515390.2:c.-84-312A>C (IL6) XP_011513692.1:n.-84-312A>C