Canonical Allele Identifier: CA1694138252

Linked Data

dbSNP Id: rs1784019996

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727157T>C , CM000669.2:g.22727157T>C GRCh38
NC_000007.13:g.22766776T>C , CM000669.1:g.22766776T>C GRCh37
NC_000007.12:g.22733301T>C NCBI36
NG_011640.1:g.5011T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+411A>G (STEAP1B)
ENST00000258743.9:c.-106T>C (IL6) ENSP00000258743.5:n.-106T>C
ENST00000401651.5:c.-143T>C (IL6) ENSP00000385718.1:n.-143T>C
ENST00000404625.5:c.-84-22T>C (IL6) ENSP00000385675.1:n.-84-22T>C
ENST00000426291.5:c.-106T>C (IL6) ENSP00000405150.1:n.-106T>C
NM_000600.3:c.-106T>C (IL6) NP_000591.1:n.-106T>C
NR_131935.1:n.53+411A>G (IL6-AS1)
XM_005249745.3:c.-106T>C (IL6) XP_005249802.1:n.-106T>C
XM_011515390.1:c.-84-22T>C (IL6) XP_011513692.1:n.-84-22T>C
NM_000600.4:c.-106T>C (IL6) NP_000591.1:n.-106T>C
NM_001318095.1:c.-143T>C (IL6) NP_001305024.1:n.-143T>C
XM_011515390.2:c.-84-22T>C (IL6) XP_011513692.1:n.-84-22T>C