Canonical Allele Identifier: CA155237169

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22725837G>C , CM000669.2:g.22725837G>C GRCh38
NC_000007.13:g.22765456G>C , CM000669.1:g.22765456G>C GRCh37
NC_000007.12:g.22731981G>C NCBI36
NG_011640.1:g.3691G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+1731C>G (STEAP1B)
NR_131935.1:n.922C>G (IL6-AS1)
XM_011515390.1:c.-506G>C (IL6) XP_011513692.1:n.-506G>C