Canonical Allele Identifier: CA15499945

Genomic Alleles

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

Transcript Alleles

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