Canonical Allele Identifier: CA1099320636

Linked Data

dbSNP Id: rs1784017121
gnomAD v3: 7-22726980-C-G
gnomAD v4: 7-22726980-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726980C>G , CM000669.2:g.22726980C>G GRCh38
NC_000007.13:g.22766599C>G , CM000669.1:g.22766599C>G GRCh37
NC_000007.12:g.22733124C>G NCBI36
NG_011640.1:g.4834C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+588G>C (STEAP1B)
ENST00000404625.5:c.-84-199C>G (IL6) ENSP00000385675.1:n.-84-199C>G
NR_131935.1:n.54-275G>C (IL6-AS1)
XM_011515390.1:c.-84-199C>G (IL6) XP_011513692.1:n.-84-199C>G
XM_011515390.2:c.-84-199C>G (IL6) XP_011513692.1:n.-84-199C>G