Canonical Allele Identifier: CA2682013347

Linked Data

gnomAD v4: 7-22727142-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727142G>T , CM000669.2:g.22727142G>T GRCh38
NC_000007.13:g.22766761G>T , CM000669.1:g.22766761G>T GRCh37
NC_000007.12:g.22733286G>T NCBI36
NG_011640.1:g.4996G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+426C>A (STEAP1B)
ENST00000404625.5:c.-84-37G>T (IL6) ENSP00000385675.1:n.-84-37G>T
NR_131935.1:n.53+426C>A (IL6-AS1)
XM_005249745.3:c.-121G>T (IL6) XP_005249802.1:n.-121G>T
XM_011515390.1:c.-84-37G>T (IL6) XP_011513692.1:n.-84-37G>T
NM_000600.4:c.-121G>T (IL6) NP_000591.1:n.-121G>T
NM_001318095.1:c.-158G>T (IL6) NP_001305024.1:n.-158G>T
XM_011515390.2:c.-84-37G>T (IL6) XP_011513692.1:n.-84-37G>T