Canonical Allele Identifier: CA2578845390

Linked Data

gnomAD v4: 7-22727211-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727211G>A , CM000669.2:g.22727211G>A GRCh38
NC_000007.13:g.22766830G>A , CM000669.1:g.22766830G>A GRCh37
NC_000007.12:g.22733355G>A NCBI36
NG_011640.1:g.5065G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.35G>A (IL6)
ENST00000258743.10:c.-52G>A (IL6) MANE Select ENSP00000258743.5:n.-52G>A
ENST00000650428.1:n.46+357C>T (STEAP1B)
ENST00000258743.9:c.-52G>A (IL6) ENSP00000258743.5:n.-52G>A
ENST00000401651.5:c.-89G>A (IL6) ENSP00000385718.1:n.-89G>A
ENST00000404625.5:c.-52G>A (IL6) ENSP00000385675.1:n.-52G>A
ENST00000426291.5:c.-52G>A (IL6) ENSP00000405150.1:n.-52G>A
ENST00000485300.1:n.12G>A (IL6)
NM_000600.3:c.-52G>A (IL6) NP_000591.1:n.-52G>A
NR_131935.1:n.53+357C>T (IL6-AS1)
XM_005249745.3:c.-52G>A (IL6) XP_005249802.1:n.-52G>A
XM_011515390.1:c.-52G>A (IL6) XP_011513692.1:n.-52G>A
XM_011515391.1:c.-89G>A (IL6) XP_011513693.1:n.-89G>A
NM_000600.4:c.-52G>A (IL6) NP_000591.1:n.-52G>A
NM_001318095.1:c.-89G>A (IL6) NP_001305024.1:n.-89G>A
XM_005249745.5:c.-52G>A (IL6) XP_005249802.1:n.-52G>A
XM_011515390.2:c.-52G>A (IL6) XP_011513692.1:n.-52G>A
NM_000600.5:c.-52G>A (IL6) MANE Select NP_000591.1:n.-52G>A
NM_001318095.2:c.-89G>A (IL6) NP_001305024.1:n.-89G>A
NM_001371096.1:c.-52G>A (IL6) NP_001358025.1:n.-52G>A