Canonical Allele Identifier: CA453973689

Linked Data

gnomAD v4: 7-22726635-G-A
MyVariant Identifiers: chr7:g.22766254G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726635G>A , CM000669.2:g.22726635G>A GRCh38
NC_000007.13:g.22766254G>A , CM000669.1:g.22766254G>A GRCh37
NC_000007.12:g.22732779G>A NCBI36
NG_011640.1:g.4489G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+933C>T (STEAP1B)
ENST00000404625.5:c.-85+377G>A (IL6) ENSP00000385675.1:n.-85+377G>A
NR_131935.1:n.124C>T (IL6-AS1)
XM_011515390.1:c.-85+377G>A (IL6) XP_011513692.1:n.-85+377G>A
XM_011515390.2:c.-85+377G>A (IL6) XP_011513692.1:n.-85+377G>A