Canonical Allele Identifier: CA2682013278

Linked Data

gnomAD v4: 7-22727089-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727089G>A , CM000669.2:g.22727089G>A GRCh38
NC_000007.13:g.22766708G>A , CM000669.1:g.22766708G>A GRCh37
NC_000007.12:g.22733233G>A NCBI36
NG_011640.1:g.4943G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+479C>T (STEAP1B)
ENST00000404625.5:c.-84-90G>A (IL6) ENSP00000385675.1:n.-84-90G>A
NR_131935.1:n.54-384C>T (IL6-AS1)
XM_005249745.3:c.-174G>A (IL6) XP_005249802.1:n.-174G>A
XM_011515390.1:c.-84-90G>A (IL6) XP_011513692.1:n.-84-90G>A
XM_011515390.2:c.-84-90G>A (IL6) XP_011513692.1:n.-84-90G>A