Canonical Allele Identifier: CA453973711

Linked Data

MyVariant Identifiers: chr7:g.22766262A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726643A>T , CM000669.2:g.22726643A>T GRCh38
NC_000007.13:g.22766262A>T , CM000669.1:g.22766262A>T GRCh37
NC_000007.12:g.22732787A>T NCBI36
NG_011640.1:g.4497A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+925T>A (STEAP1B)
ENST00000404625.5:c.-85+385A>T (IL6) ENSP00000385675.1:n.-85+385A>T
NR_131935.1:n.116T>A (IL6-AS1)
XM_011515390.1:c.-85+385A>T (IL6) XP_011513692.1:n.-85+385A>T
XM_011515390.2:c.-85+385A>T (IL6) XP_011513692.1:n.-85+385A>T