Canonical Allele Identifier: CA1099320682

Linked Data

dbSNP Id: rs1784018766
gnomAD v3: 7-22727033-A-C
gnomAD v4: 7-22727033-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727033A>C , CM000669.2:g.22727033A>C GRCh38
NC_000007.13:g.22766652A>C , CM000669.1:g.22766652A>C GRCh37
NC_000007.12:g.22733177A>C NCBI36
NG_011640.1:g.4887A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+535T>G (STEAP1B)
ENST00000404625.5:c.-84-146A>C (IL6) ENSP00000385675.1:n.-84-146A>C
NR_131935.1:n.54-328T>G (IL6-AS1)
XM_011515390.1:c.-84-146A>C (IL6) XP_011513692.1:n.-84-146A>C
XM_011515390.2:c.-84-146A>C (IL6) XP_011513692.1:n.-84-146A>C