Linked Data
MyVariant Identifiers:
chr15:g.85383416G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.84840185G>T , CM000677.2:g.84840185G>T | GRCh38 |
| NC_000015.9:g.85383416G>T , CM000677.1:g.85383416G>T | GRCh37 |
| NC_000015.8:g.83184420G>T | NCBI36 |
| NG_054748.1:g.28555G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258888.6:c.906G>T MANE Select | ENSP00000258888.6:p.Leu302= | |
| ENST00000258888.5:c.1512G>T | ENSP00000258888.5:p.Leu504= | |
| NM_020778.4:c.1512G>T | NP_065829.3:p.Leu504= | |
| NM_020778.5:c.906G>T MANE Select | NP_065829.4:p.Leu302= |