Canonical Allele Identifier: CA453973130

Linked Data

MyVariant Identifiers: chr7:g.22766061G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726442G>T , CM000669.2:g.22726442G>T GRCh38
NC_000007.13:g.22766061G>T , CM000669.1:g.22766061G>T GRCh37
NC_000007.12:g.22732586G>T NCBI36
NG_011640.1:g.4296G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+1126C>A (STEAP1B)
ENST00000404625.5:c.-85+184G>T (IL6) ENSP00000385675.1:n.-85+184G>T
NR_131935.1:n.317C>A (IL6-AS1)
XM_011515390.1:c.-85+184G>T (IL6) XP_011513692.1:n.-85+184G>T
XM_011515390.2:c.-85+184G>T (IL6) XP_011513692.1:n.-85+184G>T