Canonical Allele Identifier: CA453973140

Linked Data

MyVariant Identifiers: chr7:g.22766065A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22726446A>C , CM000669.2:g.22726446A>C GRCh38
NC_000007.13:g.22766065A>C , CM000669.1:g.22766065A>C GRCh37
NC_000007.12:g.22732590A>C NCBI36
NG_011640.1:g.4300A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+1122T>G (STEAP1B)
ENST00000404625.5:c.-85+188A>C (IL6) ENSP00000385675.1:n.-85+188A>C
NR_131935.1:n.313T>G (IL6-AS1)
XM_011515390.1:c.-85+188A>C (IL6) XP_011513692.1:n.-85+188A>C
XM_011515390.2:c.-85+188A>C (IL6) XP_011513692.1:n.-85+188A>C