Linked Data
MyVariant Identifiers:
chr12:g.52886466G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52492682G>T , CM000674.2:g.52492682G>T | GRCh38 |
| NC_000012.11:g.52886466G>T , CM000674.1:g.52886466G>T | GRCh37 |
| NC_000012.10:g.51172733G>T | NCBI36 |
| NG_008298.1:g.5716C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330722.7:c.507C>A MANE Select | ENSP00000369317.3:p.Thr169= | |
| ENST00000330722.6:c.507C>A | ENSP00000369317.3:p.Thr169= | |
| ENST00000549898.5:n.28C>A | ||
| NM_005554.3:c.507C>A | NP_005545.1:p.Thr169= | |
| NM_005554.4:c.507C>A MANE Select | NP_005545.1:p.Thr169= |