Canonical Allele Identifier: CA453973108

Linked Data

MyVariant Identifiers: chr7:g.22766054T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726435T>A , CM000669.2:g.22726435T>A GRCh38
NC_000007.13:g.22766054T>A , CM000669.1:g.22766054T>A GRCh37
NC_000007.12:g.22732579T>A NCBI36
NG_011640.1:g.4289T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+1133A>T (STEAP1B)
ENST00000404625.5:c.-85+177T>A (IL6) ENSP00000385675.1:n.-85+177T>A
NR_131935.1:n.324A>T (IL6-AS1)
XM_011515390.1:c.-85+177T>A (IL6) XP_011513692.1:n.-85+177T>A
XM_011515390.2:c.-85+177T>A (IL6) XP_011513692.1:n.-85+177T>A