Canonical Allele Identifier: CA155238350

Linked Data

dbSNP Id: rs899406081
gnomAD v3: 7-22727113-G-T
gnomAD v4: 7-22727113-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22727113G>T , CM000669.2:g.22727113G>T GRCh38
NC_000007.13:g.22766732G>T , CM000669.1:g.22766732G>T GRCh37
NC_000007.12:g.22733257G>T NCBI36
NG_011640.1:g.4967G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+455C>A (STEAP1B)
ENST00000404625.5:c.-84-66G>T (IL6) ENSP00000385675.1:n.-84-66G>T
NR_131935.1:n.54-408C>A (IL6-AS1)
XM_005249745.3:c.-150G>T (IL6) XP_005249802.1:n.-150G>T
XM_011515390.1:c.-84-66G>T (IL6) XP_011513692.1:n.-84-66G>T
XM_011515390.2:c.-84-66G>T (IL6) XP_011513692.1:n.-84-66G>T