Linked Data
MyVariant Identifiers:
chr7:g.22766111C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22726492C>T , CM000669.2:g.22726492C>T | GRCh38 |
| NC_000007.13:g.22766111C>T , CM000669.1:g.22766111C>T | GRCh37 |
| NC_000007.12:g.22732636C>T | NCBI36 |
| NG_011640.1:g.4346C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650428.1:n.46+1076G>A (STEAP1B) | ||
| ENST00000404625.5:c.-85+234C>T (IL6) | ENSP00000385675.1:n.-85+234C>T | |
| NR_131935.1:n.267G>A (IL6-AS1) | ||
| XM_011515390.1:c.-85+234C>T (IL6) | XP_011513692.1:n.-85+234C>T | |
| XM_011515390.2:c.-85+234C>T (IL6) | XP_011513692.1:n.-85+234C>T |