Canonical Allele Identifier: CA915438589

Linked Data

dbSNP Id: rs1562644651
gnomAD v2: 7-22766468-T-G
gnomAD v3: 7-22726849-T-G
gnomAD v4: 7-22726849-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726849T>G , CM000669.2:g.22726849T>G GRCh38
NC_000007.13:g.22766468T>G , CM000669.1:g.22766468T>G GRCh37
NC_000007.12:g.22732993T>G NCBI36
NG_011640.1:g.4703T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+719A>C (STEAP1B)
ENST00000404625.5:c.-84-330T>G (IL6) ENSP00000385675.1:n.-84-330T>G
NR_131935.1:n.54-144A>C (IL6-AS1)
XM_011515390.1:c.-84-330T>G (IL6) XP_011513692.1:n.-84-330T>G
XM_011515390.2:c.-84-330T>G (IL6) XP_011513692.1:n.-84-330T>G