Canonical Allele Identifier: CA155238225

Linked Data

dbSNP Id: rs925833013
gnomAD v3: 7-22726946-T-C
gnomAD v4: 7-22726946-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726946T>C , CM000669.2:g.22726946T>C GRCh38
NC_000007.13:g.22766565T>C , CM000669.1:g.22766565T>C GRCh37
NC_000007.12:g.22733090T>C NCBI36
NG_011640.1:g.4800T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+622A>G (STEAP1B)
ENST00000404625.5:c.-84-233T>C (IL6) ENSP00000385675.1:n.-84-233T>C
NR_131935.1:n.54-241A>G (IL6-AS1)
XM_011515390.1:c.-84-233T>C (IL6) XP_011513692.1:n.-84-233T>C
XM_011515390.2:c.-84-233T>C (IL6) XP_011513692.1:n.-84-233T>C