Canonical Allele Identifier: CA2682013272

Linked Data

gnomAD v4: 7-22727085-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727085T>C , CM000669.2:g.22727085T>C GRCh38
NC_000007.13:g.22766704T>C , CM000669.1:g.22766704T>C GRCh37
NC_000007.12:g.22733229T>C NCBI36
NG_011640.1:g.4939T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+483A>G (STEAP1B)
ENST00000404625.5:c.-84-94T>C (IL6) ENSP00000385675.1:n.-84-94T>C
NR_131935.1:n.54-380A>G (IL6-AS1)
XM_005249745.3:c.-178T>C (IL6) XP_005249802.1:n.-178T>C
XM_011515390.1:c.-84-94T>C (IL6) XP_011513692.1:n.-84-94T>C
XM_011515390.2:c.-84-94T>C (IL6) XP_011513692.1:n.-84-94T>C