Canonical Allele Identifier: CA1694137711
Community Standard Title: NC_000007.14:g.22725837G=

Genomic Alleles

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

Transcript Alleles

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