Canonical Allele Identifier: CA453973402

Linked Data

dbSNP Id: rs1459464244
gnomAD v4: 7-22726536-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726536C>G , CM000669.2:g.22726536C>G GRCh38
NC_000007.13:g.22766155C>G , CM000669.1:g.22766155C>G GRCh37
NC_000007.12:g.22732680C>G NCBI36
NG_011640.1:g.4390C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+1032G>C (STEAP1B)
ENST00000404625.5:c.-85+278C>G (IL6) ENSP00000385675.1:n.-85+278C>G
NR_131935.1:n.223G>C (IL6-AS1)
XM_011515390.1:c.-85+278C>G (IL6) XP_011513692.1:n.-85+278C>G
XM_011515390.2:c.-85+278C>G (IL6) XP_011513692.1:n.-85+278C>G