Canonical Allele Identifier: CA2682013370

Linked Data

gnomAD v4: 7-22727162-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727162A>C , CM000669.2:g.22727162A>C GRCh38
NC_000007.13:g.22766781A>C , CM000669.1:g.22766781A>C GRCh37
NC_000007.12:g.22733306A>C NCBI36
NG_011640.1:g.5016A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+406T>G (STEAP1B)
ENST00000258743.9:c.-101A>C (IL6) ENSP00000258743.5:n.-101A>C
ENST00000401651.5:c.-138A>C (IL6) ENSP00000385718.1:n.-138A>C
ENST00000404625.5:c.-84-17A>C (IL6) ENSP00000385675.1:n.-84-17A>C
ENST00000426291.5:c.-101A>C (IL6) ENSP00000405150.1:n.-101A>C
NM_000600.3:c.-101A>C (IL6) NP_000591.1:n.-101A>C
NR_131935.1:n.53+406T>G (IL6-AS1)
XM_005249745.3:c.-101A>C (IL6) XP_005249802.1:n.-101A>C
XM_011515390.1:c.-84-17A>C (IL6) XP_011513692.1:n.-84-17A>C
XM_011515391.1:c.-138A>C (IL6) XP_011513693.1:n.-138A>C
NM_000600.4:c.-101A>C (IL6) NP_000591.1:n.-101A>C
NM_001318095.1:c.-138A>C (IL6) NP_001305024.1:n.-138A>C
XM_011515390.2:c.-84-17A>C (IL6) XP_011513692.1:n.-84-17A>C