Linked Data
MyVariant Identifiers:
chr7:g.22766096G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22726477G>C , CM000669.2:g.22726477G>C | GRCh38 |
| NC_000007.13:g.22766096G>C , CM000669.1:g.22766096G>C | GRCh37 |
| NC_000007.12:g.22732621G>C | NCBI36 |
| NG_011640.1:g.4331G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650428.1:n.46+1091C>G (STEAP1B) | ||
| ENST00000404625.5:c.-85+219G>C (IL6) | ENSP00000385675.1:n.-85+219G>C | |
| NR_131935.1:n.282C>G (IL6-AS1) | ||
| XM_011515390.1:c.-85+219G>C (IL6) | XP_011513692.1:n.-85+219G>C | |
| XM_011515390.2:c.-85+219G>C (IL6) | XP_011513692.1:n.-85+219G>C |