Canonical Allele Identifier: CA2682013352

Linked Data

gnomAD v4: 7-22727144-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727144C>G , CM000669.2:g.22727144C>G GRCh38
NC_000007.13:g.22766763C>G , CM000669.1:g.22766763C>G GRCh37
NC_000007.12:g.22733288C>G NCBI36
NG_011640.1:g.4998C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+424G>C (STEAP1B)
ENST00000404625.5:c.-84-35C>G (IL6) ENSP00000385675.1:n.-84-35C>G
NR_131935.1:n.53+424G>C (IL6-AS1)
XM_005249745.3:c.-119C>G (IL6) XP_005249802.1:n.-119C>G
XM_011515390.1:c.-84-35C>G (IL6) XP_011513692.1:n.-84-35C>G
NM_000600.4:c.-119C>G (IL6) NP_000591.1:n.-119C>G
NM_001318095.1:c.-156C>G (IL6) NP_001305024.1:n.-156C>G
XM_011515390.2:c.-84-35C>G (IL6) XP_011513692.1:n.-84-35C>G