Canonical Allele Identifier: CA2682013355

Linked Data

gnomAD v4: 7-22727147-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727147A>G , CM000669.2:g.22727147A>G GRCh38
NC_000007.13:g.22766766A>G , CM000669.1:g.22766766A>G GRCh37
NC_000007.12:g.22733291A>G NCBI36
NG_011640.1:g.5001A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+421T>C (STEAP1B)
ENST00000258743.9:c.-116A>G (IL6) ENSP00000258743.5:n.-116A>G
ENST00000401651.5:c.-153A>G (IL6) ENSP00000385718.1:n.-153A>G
ENST00000404625.5:c.-84-32A>G (IL6) ENSP00000385675.1:n.-84-32A>G
ENST00000426291.5:c.-116A>G (IL6) ENSP00000405150.1:n.-116A>G
NM_000600.3:c.-116A>G (IL6) NP_000591.1:n.-116A>G
NR_131935.1:n.53+421T>C (IL6-AS1)
XM_005249745.3:c.-116A>G (IL6) XP_005249802.1:n.-116A>G
XM_011515390.1:c.-84-32A>G (IL6) XP_011513692.1:n.-84-32A>G
NM_000600.4:c.-116A>G (IL6) NP_000591.1:n.-116A>G
NM_001318095.1:c.-153A>G (IL6) NP_001305024.1:n.-153A>G
XM_011515390.2:c.-84-32A>G (IL6) XP_011513692.1:n.-84-32A>G