Canonical Allele Identifier: CA2682013375

Linked Data

gnomAD v4: 7-22727163-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727163C>T , CM000669.2:g.22727163C>T GRCh38
NC_000007.13:g.22766782C>T , CM000669.1:g.22766782C>T GRCh37
NC_000007.12:g.22733307C>T NCBI36
NG_011640.1:g.5017C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+405G>A (STEAP1B)
ENST00000258743.9:c.-100C>T (IL6) ENSP00000258743.5:n.-100C>T
ENST00000401651.5:c.-137C>T (IL6) ENSP00000385718.1:n.-137C>T
ENST00000404625.5:c.-84-16C>T (IL6) ENSP00000385675.1:n.-84-16C>T
ENST00000426291.5:c.-100C>T (IL6) ENSP00000405150.1:n.-100C>T
NM_000600.3:c.-100C>T (IL6) NP_000591.1:n.-100C>T
NR_131935.1:n.53+405G>A (IL6-AS1)
XM_005249745.3:c.-100C>T (IL6) XP_005249802.1:n.-100C>T
XM_011515390.1:c.-84-16C>T (IL6) XP_011513692.1:n.-84-16C>T
XM_011515391.1:c.-137C>T (IL6) XP_011513693.1:n.-137C>T
NM_000600.4:c.-100C>T (IL6) NP_000591.1:n.-100C>T
NM_001318095.1:c.-137C>T (IL6) NP_001305024.1:n.-137C>T
XM_005249745.5:c.-100C>T (IL6) XP_005249802.1:n.-100C>T
XM_011515390.2:c.-84-16C>T (IL6) XP_011513692.1:n.-84-16C>T