Canonical Allele Identifier: CA2682013312

Linked Data

gnomAD v4: 7-22727120-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727120C>G , CM000669.2:g.22727120C>G GRCh38
NC_000007.13:g.22766739C>G , CM000669.1:g.22766739C>G GRCh37
NC_000007.12:g.22733264C>G NCBI36
NG_011640.1:g.4974C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+448G>C (STEAP1B)
ENST00000404625.5:c.-84-59C>G (IL6) ENSP00000385675.1:n.-84-59C>G
NR_131935.1:n.54-415G>C (IL6-AS1)
XM_005249745.3:c.-143C>G (IL6) XP_005249802.1:n.-143C>G
XM_011515390.1:c.-84-59C>G (IL6) XP_011513692.1:n.-84-59C>G
XM_011515390.2:c.-84-59C>G (IL6) XP_011513692.1:n.-84-59C>G